ENST00000326003.7:c.439G>T
MANE Select
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ENSP00000314151.1:p.Ala147Ser
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ENST00000326003.6:c.439G>T
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ENSP00000314151.1:p.Ala147Ser
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ENST00000360617.7:c.439G>T
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ENSP00000353829.2:p.Ala147Ser
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ENST00000422986.6:c.*95G>T
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ENSP00000393628.2:n.*95G>T
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ENST00000593997.5:c.439G>T
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ENSP00000472907.1:p.Ala147Ser
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ENST00000595392.5:c.353-38G>T
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ENSP00000468912.1:n.353-38G>T
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ENST00000595952.5:c.310G>T
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ENSP00000471155.1:p.Ala104Ser
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ENST00000596185.5:c.*547G>T
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ENSP00000471648.1:n.*547G>T
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ENST00000596333.1:n.474G>T
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|
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ENST00000597286.5:c.328G>T
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ENSP00000470523.1:p.Ala110Ser
|
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ENST00000597483.5:c.310G>T
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ENSP00000472411.1:p.Ala104Ser
|
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ENST00000598145.1:c.423G>T
|
|
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ENST00000601349.5:n.1718G>T
|
|
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ENST00000601503.5:c.382G>T
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ENSP00000472213.1:p.Ala128Ser
|
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ENST00000601812.1:n.871G>T
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|
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ENST00000617027.4:c.354-38G>T
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ENSP00000483513.1:n.354-38G>T
|
|
NM_001030047.1:c.439G>T
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NP_001025218.1:p.Ala147Ser
|
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NM_001030048.1:c.310G>T
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NP_001025219.1:p.Ala104Ser
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NM_001648.2:c.439G>T
MANE Select
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NP_001639.1:p.Ala147Ser
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XM_011526923.1:c.439G>T
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XP_011525225.1:p.Ala147Ser
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XM_011526924.1:c.439G>T
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XP_011525226.1:p.Ala147Ser
|
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XR_935817.1:n.474G>T
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