ENST00000309383.6:c.2138T>A
MANE Select
|
ENSP00000310649.1:p.Leu713His
|
|
ENST00000309383.5:c.2138T>A
|
ENSP00000310649.1:p.Leu713His
|
|
ENST00000326848.7:c.1223T>A
|
ENSP00000320853.7:p.Leu408His
|
|
ENST00000590333.5:c.2186T>A
|
ENSP00000468190.1:p.Leu729His
|
|
NM_032430.1:c.2138T>A
|
NP_115806.1:p.Leu713His
|
|
XM_005259327.2:c.1868T>A
|
XP_005259384.1:p.Leu623His
|
|
XM_011527395.1:c.1895T>A
|
XP_011525697.1:p.Leu632His
|
|
XR_430213.2:n.2121T>A
|
|
|
XM_005259327.3:c.1868T>A
|
XP_005259384.1:p.Leu623His
|
|
XM_011527395.2:c.1610T>A
|
XP_011525697.2:p.Leu537His
|
|
XM_024451739.1:c.1913T>A
|
XP_024307507.1:p.Leu638His
|
|
XR_430213.4:n.2419T>A
|
|
|
NM_032430.2:c.2138T>A
MANE Select
|
NP_115806.1:p.Leu713His
|
|