ENST00000309383.6:c.2114T>G
MANE Select
|
ENSP00000310649.1:p.Val705Gly
|
|
ENST00000309383.5:c.2114T>G
|
ENSP00000310649.1:p.Val705Gly
|
|
ENST00000326848.7:c.1199T>G
|
ENSP00000320853.7:p.Val400Gly
|
|
ENST00000590333.5:c.2162T>G
|
ENSP00000468190.1:p.Val721Gly
|
|
NM_032430.1:c.2114T>G
|
NP_115806.1:p.Val705Gly
|
|
XM_005259327.2:c.1844T>G
|
XP_005259384.1:p.Val615Gly
|
|
XM_011527395.1:c.1871T>G
|
XP_011525697.1:p.Val624Gly
|
|
XR_430213.2:n.2097T>G
|
|
|
XM_005259327.3:c.1844T>G
|
XP_005259384.1:p.Val615Gly
|
|
XM_011527395.2:c.1586T>G
|
XP_011525697.2:p.Val529Gly
|
|
XM_024451739.1:c.1889T>G
|
XP_024307507.1:p.Val630Gly
|
|
XR_430213.4:n.2395T>G
|
|
|
NM_032430.2:c.2114T>G
MANE Select
|
NP_115806.1:p.Val705Gly
|
|