ENST00000309383.6:c.2165T>C
MANE Select
|
ENSP00000310649.1:p.Val722Ala
|
|
ENST00000309383.5:c.2165T>C
|
ENSP00000310649.1:p.Val722Ala
|
|
ENST00000326848.7:c.1250T>C
|
ENSP00000320853.7:p.Val417Ala
|
|
ENST00000590333.5:c.2213T>C
|
ENSP00000468190.1:p.Val738Ala
|
|
NM_032430.1:c.2165T>C
|
NP_115806.1:p.Val722Ala
|
|
XM_005259327.2:c.1895T>C
|
XP_005259384.1:p.Val632Ala
|
|
XM_011527395.1:c.1922T>C
|
XP_011525697.1:p.Val641Ala
|
|
XR_430213.2:n.2148T>C
|
|
|
XM_005259327.3:c.1895T>C
|
XP_005259384.1:p.Val632Ala
|
|
XM_011527395.2:c.1637T>C
|
XP_011525697.2:p.Val546Ala
|
|
XM_024451739.1:c.1940T>C
|
XP_024307507.1:p.Val647Ala
|
|
XR_430213.4:n.2446T>C
|
|
|
NM_032430.2:c.2165T>C
MANE Select
|
NP_115806.1:p.Val722Ala
|
|