ENST00000281928.9:c.2675T>C
MANE Select
|
ENSP00000281928.3:p.Val892Ala
|
|
ENST00000548743.2:c.2645T>C
|
ENSP00000448553.2:p.Val882Ala
|
|
ENST00000549786.2:c.2103T>C
|
|
|
ENST00000647927.1:n.3048T>C
|
|
|
ENST00000648173.1:n.1470T>C
|
|
|
ENST00000648379.1:n.1043T>C
|
|
|
ENST00000648737.1:n.2439T>C
|
|
|
ENST00000648916.1:n.686T>C
|
|
|
ENST00000649607.1:c.859T>C
|
|
|
ENST00000650226.1:c.2675T>C
|
ENSP00000496981.1:p.Val892Ala
|
|
ENST00000281928.7:c.2675T>C
|
ENSP00000281928.3:p.Val892Ala
|
|
NM_015335.4:c.2675T>C
|
NP_056150.1:p.Val892Ala
|
|
XM_011538080.1:c.2675T>C
|
XP_011536382.1:p.Val892Ala
|
|
XM_011538081.1:c.2672T>C
|
XP_011536383.1:p.Val891Ala
|
|
XM_011538082.1:c.2645T>C
|
XP_011536384.1:p.Val882Ala
|
|
XM_011538080.2:c.2675T>C
|
XP_011536382.1:p.Val892Ala
|
|
XM_011538081.2:c.2672T>C
|
XP_011536383.1:p.Val891Ala
|
|
XM_011538082.2:c.2645T>C
|
XP_011536384.1:p.Val882Ala
|
|
XM_017019090.1:c.2672T>C
|
XP_016874579.1:p.Val891Ala
|
|
NM_015335.5:c.2675T>C
MANE Select
|
NP_056150.1:p.Val892Ala
|
|