ENST00000333213.11:c.811G>T
MANE Select
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ENSP00000327487.6:p.Ala271Ser
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ENST00000434205.8:c.508G>T
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ENSP00000406559.4:p.Ala170Ser
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ENST00000545228.3:c.811G>T
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ENSP00000438169.3:p.Ala271Ser
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ENST00000579449.2:n.610G>T
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ENST00000580013.6:n.1014G>T
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ENST00000583818.2:c.865G>T
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ENSP00000461928.2:n.865G>T
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ENST00000679370.1:n.1392G>T
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ENST00000679429.1:c.*269G>T
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ENSP00000505403.1:n.*269G>T
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ENST00000679443.1:n.880G>T
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ENST00000679782.1:c.811G>T
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ENSP00000505995.1:p.Ala271Ser
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ENST00000679919.1:n.880G>T
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|
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ENST00000679928.1:c.*422G>T
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ENSP00000506071.1:n.*422G>T
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ENST00000680528.1:n.836G>T
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|
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ENST00000680999.1:c.811G>T
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ENSP00000504984.1:p.Ala271Ser
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ENST00000681282.1:c.*57G>T
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ENSP00000506339.1:n.*57G>T
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ENST00000333213.10:c.811G>T
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ENSP00000327487.6:p.Ala271Ser
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ENST00000578415.1:c.771G>T
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ENST00000583173.5:c.459-115G>T
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ENSP00000463619.1:n.459-115G>T
|
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ENST00000583818.1:c.760G>T
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ENSP00000461928.1:n.760G>T
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NM_207346.2:c.811G>T
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NP_997229.2:p.Ala271Ser
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XM_005257229.2:c.811G>T
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XP_005257286.1:p.Ala271Ser
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XM_006721821.2:c.508G>T
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XP_006721884.1:p.Ala170Ser
|
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XM_011524616.1:c.811G>T
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XP_011522918.1:p.Ala271Ser
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XM_011524617.1:c.811G>T
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XP_011522919.1:p.Ala271Ser
|
|
XM_011524618.1:c.811G>T
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XP_011522920.1:p.Ala271Ser
|
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XR_243646.2:n.841G>T
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XM_005257229.4:c.811G>T
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XP_005257286.1:p.Ala271Ser
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XR_243646.4:n.847G>T
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|
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NM_207346.3:c.811G>T
MANE Select
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NP_997229.2:p.Ala271Ser
|
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