ENST00000320185.7:c.227G>C
MANE Select
|
ENSP00000321797.2:p.Ser76Thr
|
|
ENST00000618991.5:c.-86G>C
|
ENSP00000484420.1:n.-86G>C
|
|
ENST00000344255.8:c.194G>C
|
ENSP00000340039.3:p.Ser65Thr
|
|
ENST00000320185.6:c.227G>C
|
ENSP00000321797.2:p.Ser76Thr
|
|
ENST00000344255.7:c.194G>C
|
ENSP00000340039.3:p.Ser65Thr
|
|
ENST00000346714.7:c.107G>C
|
ENSP00000344306.3:p.Ser36Thr
|
|
ENST00000347978.2:c.140G>C
|
ENSP00000321945.2:p.Ser47Thr
|
|
ENST00000469792.6:c.*191G>C
|
ENSP00000473299.1:n.*191G>C
|
|
ENST00000485728.1:n.103G>C
|
|
|
ENST00000618991.4:c.-86G>C
|
ENSP00000484420.1:n.-86G>C
|
|
NM_001206389.1:c.-86G>C
|
NP_001193318.1:n.-86G>C
|
|
NM_006119.4:c.140G>C
|
NP_006110.1:p.Ser47Thr
|
|
NM_033163.3:c.227G>C
|
NP_149353.1:p.Ser76Thr
|
|
NM_033164.3:c.194G>C
|
NP_149354.1:p.Ser65Thr
|
|
NM_033165.3:c.107G>C
|
NP_149355.1:p.Ser36Thr
|
|
XM_011539509.1:c.149G>C
|
XP_011537811.1:p.Ser50Thr
|
|
NM_006119.5:c.140G>C
|
NP_006110.1:p.Ser47Thr
|
|
NM_033163.4:c.227G>C
|
NP_149353.1:p.Ser76Thr
|
|
NM_033164.4:c.194G>C
|
NP_149354.1:p.Ser65Thr
|
|
NM_033165.4:c.107G>C
|
NP_149355.1:p.Ser36Thr
|
|
NM_001206389.2:c.-86G>C
|
NP_001193318.1:n.-86G>C
|
|
NM_006119.6:c.140G>C
|
NP_006110.1:p.Ser47Thr
|
|
NM_033163.5:c.227G>C
MANE Select
|
NP_149353.1:p.Ser76Thr
|
|
NM_033165.5:c.107G>C
|
NP_149355.1:p.Ser36Thr
|
|