ENST00000318158.11:c.552G>A
MANE Select
|
ENSP00000313432.6:p.Gly184=
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ENST00000318158.10:c.552G>A
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ENSP00000313432.6:p.Gly184=
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|
ENST00000377824.8:n.589G>A
|
|
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ENST00000460882.5:n.579G>A
|
|
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ENST00000480596.5:n.1253G>A
|
|
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ENST00000482603.1:n.5G>A
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|
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ENST00000491488.5:n.257G>A
|
|
|
ENST00000494290.1:c.123G>A
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ENSP00000432021.1:p.Gly41=
|
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ENST00000497693.1:n.2085G>A
|
|
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ENST00000607784.1:c.552G>A
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ENSP00000475569.1:p.Gly184=
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NM_012203.1:c.552G>A
|
NP_036335.1:p.Gly184=
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XM_005251631.1:c.231G>A
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XP_005251688.1:p.Gly77=
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XM_011518073.1:c.150G>A
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XP_011516375.1:p.Gly50=
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|
XR_929374.1:n.997G>A
|
|
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XM_017015320.2:c.552G>A
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XP_016870809.1:p.Gly184=
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|
XM_017015321.2:c.552G>A
|
XP_016870810.1:p.Gly184=
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|
XM_017015323.2:c.150G>A
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XP_016870812.1:p.Gly50=
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XM_024447716.1:c.825G>A
|
XP_024303484.1:p.Gly275=
|
|
XM_024447717.1:c.825G>A
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XP_024303485.1:p.Gly275=
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XR_002956828.1:n.840G>A
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|
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XR_002956829.1:n.840G>A
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XR_002956830.1:n.611G>A
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XR_002956831.1:n.286G>A
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XR_002956832.1:n.971G>A
|
|
|
NM_012203.2:c.552G>A
MANE Select
|
NP_036335.1:p.Gly184=
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