ENST00000267845.8:c.1775T>G
MANE Select
|
ENSP00000267845.3:p.Val592Gly
|
|
ENST00000267845.7:c.1775T>G
|
ENSP00000267845.3:p.Val592Gly
|
|
ENST00000543581.5:c.1676T>G
|
ENSP00000440252.1:p.Val559Gly
|
|
ENST00000559816.1:n.1519T>G
|
|
|
NM_001306146.1:c.1676T>G
|
NP_001293075.1:p.Val559Gly
|
|
NM_002112.3:c.1775T>G
|
NP_002103.2:p.Val592Gly
|
|
XM_011521479.1:c.1538T>G
|
XP_011519781.1:p.Val513Gly
|
|
XM_011521480.1:c.1343T>G
|
XP_011519782.1:p.Val448Gly
|
|
XM_017022094.1:c.1880T>G
|
XP_016877583.1:p.Val627Gly
|
|
XM_017022095.1:c.1781T>G
|
XP_016877584.1:p.Val594Gly
|
|
XM_017022096.1:c.1652T>G
|
XP_016877585.1:p.Val551Gly
|
|
XM_017022097.1:c.1643T>G
|
XP_016877586.1:p.Val548Gly
|
|
XM_017022098.1:c.1448T>G
|
XP_016877587.1:p.Val483Gly
|
|
NM_002112.4:c.1775T>G
MANE Select
|
NP_002103.2:p.Val592Gly
|
|
NM_001306146.2:c.1676T>G
|
NP_001293075.1:p.Val559Gly
|
|