ENST00000309383.6:c.2157G>C
MANE Select
|
ENSP00000310649.1:p.Gln719His
|
|
ENST00000309383.5:c.2157G>C
|
ENSP00000310649.1:p.Gln719His
|
|
ENST00000326848.7:c.1242G>C
|
ENSP00000320853.7:p.Gln414His
|
|
ENST00000590333.5:c.2205G>C
|
ENSP00000468190.1:p.Gln735His
|
|
NM_032430.1:c.2157G>C
|
NP_115806.1:p.Gln719His
|
|
XM_005259327.2:c.1887G>C
|
XP_005259384.1:p.Gln629His
|
|
XM_011527395.1:c.1914G>C
|
XP_011525697.1:p.Gln638His
|
|
XR_430213.2:n.2140G>C
|
|
|
XM_005259327.3:c.1887G>C
|
XP_005259384.1:p.Gln629His
|
|
XM_011527395.2:c.1629G>C
|
XP_011525697.2:p.Gln543His
|
|
XM_024451739.1:c.1932G>C
|
XP_024307507.1:p.Gln644His
|
|
XR_430213.4:n.2438G>C
|
|
|
NM_032430.2:c.2157G>C
MANE Select
|
NP_115806.1:p.Gln719His
|
|