ENST00000260191.8:c.404T>C
MANE Select
|
ENSP00000260191.2:p.Val135Ala
|
|
ENST00000260191.7:c.404T>C
|
ENSP00000260191.2:p.Val135Ala
|
|
ENST00000260191.6:c.404T>C
|
ENSP00000260191.2:p.Val135Ala
|
|
ENST00000537778.5:c.371T>C
|
ENSP00000443118.1:p.Val124Ala
|
|
ENST00000543092.1:c.190T>C
|
|
|
NM_006028.4:c.404T>C
|
NP_006019.1:p.Val135Ala
|
|
XM_011543063.1:c.371T>C
|
XP_011541365.1:p.Val124Ala
|
|
XM_011543064.1:c.203T>C
|
XP_011541366.1:p.Val68Ala
|
|
XM_011543065.1:c.197T>C
|
XP_011541367.1:p.Val66Ala
|
|
XM_011543066.1:c.371T>C
|
XP_011541368.1:p.Val124Ala
|
|
NM_001363563.1:c.371T>C
|
NP_001350492.1:p.Val124Ala
|
|
XM_017018552.2:c.197T>C
|
XP_016874041.1:p.Val66Ala
|
|
XM_024448767.1:c.110T>C
|
XP_024304535.1:p.Val37Ala
|
|
XR_001748034.2:n.655T>C
|
|
|
NM_001363563.2:c.371T>C
|
NP_001350492.1:p.Val124Ala
|
|
NM_006028.5:c.404T>C
MANE Select
|
NP_006019.1:p.Val135Ala
|
|