ENST00000400723.8:c.163+81T>C
MANE Select
|
ENSP00000383558.3:n.163+81T>C
|
|
ENST00000400723.7:c.163+81T>C
|
ENSP00000383558.3:n.163+81T>C
|
|
ENST00000570996.5:c.163+81T>C
|
ENSP00000460976.1:n.163+81T>C
|
|
ENST00000572185.1:n.539T>C
|
|
|
ENST00000573428.1:c.163+81T>C
|
ENSP00000458930.1:n.163+81T>C
|
|
ENST00000574283.2:n.178T>C
|
|
|
NM_000160.4:c.163+81T>C
|
NP_000151.1:n.163+81T>C
|
|
XM_006722277.1:c.163+81T>C
|
XP_006722340.1:n.163+81T>C
|
|
XM_011523539.1:c.18T>C
|
XP_011521841.1:p.Gly6=
|
|
XM_011523540.1:c.-273T>C
|
XP_011521842.1:n.-273T>C
|
|
XM_017024446.1:c.157+81T>C
|
XP_016879935.1:n.157+81T>C
|
|
XM_017024447.1:c.-273T>C
|
XP_016879936.1:n.-273T>C
|
|
NM_000160.5:c.163+81T>C
MANE Select
|
NP_000151.1:n.163+81T>C
|
|