ENST00000504286.2:c.323G>C
|
ENSP00000518753.1:p.Gly108Ala
|
|
ENST00000510531.6:c.*444G>C
|
ENSP00000425330.1:n.*444G>C
|
|
ENST00000274192.7:c.323G>C
MANE Select
|
ENSP00000274192.5:p.Gly108Ala
|
|
ENST00000274192.6:c.323G>C
|
ENSP00000274192.5:p.Gly108Ala
|
|
ENST00000504286.1:n.444G>C
|
|
|
ENST00000510531.5:c.*444G>C
|
ENSP00000425330.1:n.*444G>C
|
|
ENST00000513117.1:c.294-4207G>C
|
ENSP00000421342.1:n.294-4207G>C
|
|
NM_001047.2:c.323G>C
|
NP_001038.1:p.Gly108Ala
|
|
XM_011514103.1:c.320-4207G>C
|
XP_011512405.1:n.320-4207G>C
|
|
NM_001047.3:c.323G>C
|
NP_001038.1:p.Gly108Ala
|
|
NM_001324322.1:c.320-4207G>C
|
NP_001311251.1:n.320-4207G>C
|
|
NM_001324323.1:c.104G>C
|
NP_001311252.1:p.Gly35Ala
|
|
NR_136739.1:n.578G>C
|
|
|
NM_001047.4:c.323G>C
MANE Select
|
NP_001038.1:p.Gly108Ala
|
|
NM_001324322.2:c.320-4207G>C
|
NP_001311251.1:n.320-4207G>C
|
|
NM_001324323.2:c.104G>C
|
NP_001311252.1:p.Gly35Ala
|
|
NR_136739.2:n.460G>C
|
|
|