ENST00000399503.4:c.2479G=
MANE Select
|
ENSP00000382423.3:p.Val827=
|
|
ENST00000399503.3:c.2479G=
|
ENSP00000382423.3:p.Val827=
|
|
NM_005921.1:c.2479G=
|
NP_005912.1:p.Val827=
|
|
XM_005248519.3:c.2101G=
|
XP_005248576.2:p.Val701=
|
|
XM_011543406.1:c.2224G=
|
XP_011541708.1:p.Val742=
|
|
XM_011543407.1:c.2200G=
|
XP_011541709.1:p.Val734=
|
|
XM_011543408.1:c.2479G=
|
XP_011541710.1:p.Val827=
|
|
XM_017009484.1:c.2068G=
|
XP_016864973.1:p.Val690=
|
|
XM_017009485.1:c.1990G=
|
XP_016864974.1:p.Val664=
|
|
XR_001742068.2:n.2510G=
|
|
|
NM_005921.2:c.2479G=
MANE Select
|
NP_005912.1:p.Val827=
|
|