ENST00000447944.7:c.1145G>T
MANE Select
|
ENSP00000400646.2:p.Gly382Val
|
|
ENST00000260604.8:c.*700G>T
|
ENSP00000260604.4:n.*700G>T
|
|
ENST00000415374.5:c.1145G>T
|
ENSP00000393953.1:p.Gly382Val
|
|
ENST00000415489.1:c.219G>T
|
|
|
ENST00000447944.6:c.1145G>T
|
ENSP00000400646.2:p.Gly382Val
|
|
NM_033109.4:c.1145G>T
|
NP_149100.2:p.Gly382Val
|
|
XM_005264629.1:c.905G>T
|
XP_005264686.1:p.Gly302Val
|
|
XM_011533142.1:c.1145G>T
|
XP_011531444.1:p.Gly382Val
|
|
XM_005264629.2:c.905G>T
|
XP_005264686.1:p.Gly302Val
|
|
XM_017005172.1:c.905G>T
|
XP_016860661.1:p.Gly302Val
|
|
XR_001739010.1:n.1175G>T
|
|
|
NM_033109.5:c.1145G>T
MANE Select
|
NP_149100.2:p.Gly382Val
|
|