ENST00000309383.6:c.2169G>T
MANE Select
|
ENSP00000310649.1:p.Gln723His
|
|
ENST00000309383.5:c.2169G>T
|
ENSP00000310649.1:p.Gln723His
|
|
ENST00000326848.7:c.1254G>T
|
ENSP00000320853.7:p.Gln418His
|
|
ENST00000590333.5:c.2217G>T
|
ENSP00000468190.1:p.Gln739His
|
|
NM_032430.1:c.2169G>T
|
NP_115806.1:p.Gln723His
|
|
XM_005259327.2:c.1899G>T
|
XP_005259384.1:p.Gln633His
|
|
XM_011527395.1:c.1926G>T
|
XP_011525697.1:p.Gln642His
|
|
XR_430213.2:n.2152G>T
|
|
|
XM_005259327.3:c.1899G>T
|
XP_005259384.1:p.Gln633His
|
|
XM_011527395.2:c.1641G>T
|
XP_011525697.2:p.Gln547His
|
|
XM_024451739.1:c.1944G>T
|
XP_024307507.1:p.Gln648His
|
|
XR_430213.4:n.2450G>T
|
|
|
NM_032430.2:c.2169G>T
MANE Select
|
NP_115806.1:p.Gln723His
|
|