ENST00000357578.8:c.587G>A
MANE Select
|
ENSP00000350191.3:p.Gly196Asp
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ENST00000672352.1:c.350G>A
|
ENSP00000500876.1:p.Gly117Asp
|
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ENST00000672557.1:c.505G>A
|
|
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ENST00000672652.1:c.508G>A
|
|
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ENST00000675422.1:n.1347G>A
|
|
|
ENST00000348925.2:c.587G>A
|
ENSP00000314649.3:p.Gly196Asp
|
|
ENST00000357578.7:c.587G>A
|
ENSP00000350191.3:p.Gly196Asp
|
|
ENST00000491546.5:c.503G>A
|
ENSP00000417687.1:p.Gly168Asp
|
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NM_001080.3:c.587G>A
MANE Select
|
NP_001071.1:p.Gly196Asp
|
|
NM_170740.1:c.587G>A
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NP_733936.1:p.Gly196Asp
|
|
NM_001368954.1:c.587G>A
|
NP_001355883.1:p.Gly196Asp
|
|