ENST00000267845.8:c.1811T>G
MANE Select
|
ENSP00000267845.3:p.Val604Gly
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ENST00000267845.7:c.1811T>G
|
ENSP00000267845.3:p.Val604Gly
|
|
ENST00000543581.5:c.1712T>G
|
ENSP00000440252.1:p.Val571Gly
|
|
ENST00000559816.1:n.1555T>G
|
|
|
NM_001306146.1:c.1712T>G
|
NP_001293075.1:p.Val571Gly
|
|
NM_002112.3:c.1811T>G
|
NP_002103.2:p.Val604Gly
|
|
XM_011521479.1:c.1574T>G
|
XP_011519781.1:p.Val525Gly
|
|
XM_011521480.1:c.1379T>G
|
XP_011519782.1:p.Val460Gly
|
|
XM_017022094.1:c.1916T>G
|
XP_016877583.1:p.Val639Gly
|
|
XM_017022095.1:c.1817T>G
|
XP_016877584.1:p.Val606Gly
|
|
XM_017022096.1:c.1688T>G
|
XP_016877585.1:p.Val563Gly
|
|
XM_017022097.1:c.1679T>G
|
XP_016877586.1:p.Val560Gly
|
|
XM_017022098.1:c.1484T>G
|
XP_016877587.1:p.Val495Gly
|
|
NM_002112.4:c.1811T>G
MANE Select
|
NP_002103.2:p.Val604Gly
|
|
NM_001306146.2:c.1712T>G
|
NP_001293075.1:p.Val571Gly
|
|