ENST00000559133.6:c.6530G>T
|
ENSP00000453958.2:p.Gly2177Val
|
|
ENST00000674301.2:c.6530G>T
|
ENSP00000501333.2:p.Gly2177Val
|
|
ENST00000682170.1:n.139G>T
|
|
|
ENST00000316623.10:c.6530G>T
MANE Select
|
ENSP00000325527.5:p.Gly2177Val
|
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ENST00000674301.1:c.1529G>T
|
ENSP00000501333.1:p.Gly510Val
|
|
ENST00000316623.9:c.6530G>T
|
ENSP00000325527.5:p.Gly2177Val
|
|
ENST00000537463.6:c.*2293G>T
|
ENSP00000440294.2:n.*2293G>T
|
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ENST00000559133.5:c.1837G>T
|
|
|
NM_000138.4:c.6530G>T , LRG_778t1:c.6530G>T
|
NP_000129.3:p.Gly2177Val
|
|
NM_000138.5:c.6530G>T
MANE Select
|
NP_000129.3:p.Gly2177Val
|
|