ENST00000309383.6:c.2117T>C
MANE Select
|
ENSP00000310649.1:p.Val706Ala
|
|
ENST00000309383.5:c.2117T>C
|
ENSP00000310649.1:p.Val706Ala
|
|
ENST00000326848.7:c.1202T>C
|
ENSP00000320853.7:p.Val401Ala
|
|
ENST00000590333.5:c.2165T>C
|
ENSP00000468190.1:p.Val722Ala
|
|
NM_032430.1:c.2117T>C
|
NP_115806.1:p.Val706Ala
|
|
XM_005259327.2:c.1847T>C
|
XP_005259384.1:p.Val616Ala
|
|
XM_011527395.1:c.1874T>C
|
XP_011525697.1:p.Val625Ala
|
|
XR_430213.2:n.2100T>C
|
|
|
XM_005259327.3:c.1847T>C
|
XP_005259384.1:p.Val616Ala
|
|
XM_011527395.2:c.1589T>C
|
XP_011525697.2:p.Val530Ala
|
|
XM_024451739.1:c.1892T>C
|
XP_024307507.1:p.Val631Ala
|
|
XR_430213.4:n.2398T>C
|
|
|
NM_032430.2:c.2117T>C
MANE Select
|
NP_115806.1:p.Val706Ala
|
|