ENST00000262304.9:c.12323G>C
MANE Select
|
ENSP00000262304.4:p.Trp4108Ser
|
|
ENST00000262304.8:c.12323G>C
|
ENSP00000262304.4:p.Trp4108Ser
|
|
ENST00000423118.5:c.12320G>C
|
ENSP00000399501.1:p.Trp4107Ser
|
|
ENST00000472577.1:n.351G>C
|
|
|
NM_000296.3:c.12320G>C
|
NP_000287.3:p.Trp4107Ser
|
|
NM_001009944.2:c.12323G>C
|
NP_001009944.2:p.Trp4108Ser
|
|
XM_005255370.2:c.9278G>C
|
XP_005255427.1:p.Trp3093Ser
|
|
XM_011522525.1:c.12401G>C
|
XP_011520827.1:p.Trp4134Ser
|
|
XM_011522526.1:c.12398G>C
|
XP_011520828.1:p.Trp4133Ser
|
|
XM_011522527.1:c.12383G>C
|
XP_011520829.1:p.Trp4128Ser
|
|
XM_011522528.1:c.12377G>C
|
XP_011520830.1:p.Trp4126Ser
|
|
XM_011522529.1:c.12374G>C
|
XP_011520831.1:p.Trp4125Ser
|
|
XM_011522530.1:c.12347G>C
|
XP_011520832.1:p.Trp4116Ser
|
|
XM_011522531.1:c.12329G>C
|
XP_011520833.1:p.Trp4110Ser
|
|
XM_011522532.1:c.12275G>C
|
XP_011520834.1:p.Trp4092Ser
|
|
XM_011522533.1:c.12194G>C
|
XP_011520835.1:p.Trp4065Ser
|
|
XM_011522534.1:c.12137G>C
|
XP_011520836.1:p.Trp4046Ser
|
|
XM_011522535.1:c.10223G>C
|
XP_011520837.1:p.Trp3408Ser
|
|
XM_011522537.1:c.9401G>C
|
XP_011520839.1:p.Trp3134Ser
|
|
XR_932867.1:n.12241G>C
|
|
|
XM_005255370.3:c.9278G>C
|
XP_005255427.1:p.Trp3093Ser
|
|
XM_011522528.3:c.12377G>C
|
XP_011520830.1:p.Trp4126Ser
|
|
XM_011522529.2:c.12374G>C
|
XP_011520831.1:p.Trp4125Ser
|
|
XM_011522537.2:c.9401G>C
|
XP_011520839.1:p.Trp3134Ser
|
|
XM_024450298.1:c.12443G>C
|
XP_024306066.1:p.Trp4148Ser
|
|
XM_024450299.1:c.12371G>C
|
XP_024306067.1:p.Trp4124Ser
|
|
XM_024450300.1:c.12233G>C
|
XP_024306068.1:p.Trp4078Ser
|
|
XM_024450301.1:c.10319G>C
|
XP_024306069.1:p.Trp3440Ser
|
|
NM_000296.4:c.12320G>C
|
NP_000287.4:p.Trp4107Ser
|
|
NM_001009944.3:c.12323G>C
MANE Select
|
NP_001009944.3:p.Trp4108Ser
|
|