|
ENST00000375687.10:c.3586G>T
MANE Select
|
ENSP00000364839.4:p.Ala1196Ser
|
|
|
ENST00000646985.1:c.3403G>T
|
ENSP00000495053.1:p.Ala1135Ser
|
|
|
ENST00000647223.1:n.5939G>T
|
|
|
|
ENST00000651418.1:c.1869+1717G>T
|
ENSP00000499150.1:n.1869+1717G>T
|
|
|
ENST00000306058.9:c.3571G>T
|
ENSP00000305119.5:p.Ala1191Ser
|
|
|
ENST00000375687.8:c.3586G>T
|
ENSP00000364839.4:p.Ala1196Ser
|
|
|
ENST00000613218.4:c.3586G>T
|
ENSP00000480487.1:p.Ala1196Ser
|
|
|
ENST00000620121.4:c.3586G>T
|
ENSP00000481978.1:p.Ala1196Ser
|
|
|
NM_015338.5:c.3586G>T , LRG_630t1:c.3586G>T
|
NP_056153.2:p.Ala1196Ser
|
|
|
XM_006723727.2:c.3583G>T
|
XP_006723790.1:p.Ala1195Ser
|
|
|
XM_006723728.2:c.3556G>T
|
XP_006723791.1:p.Ala1186Ser
|
|
|
XM_006723730.2:c.3502G>T
|
XP_006723793.1:p.Ala1168Ser
|
|
|
XM_006723732.2:c.3403G>T
|
XP_006723795.1:p.Ala1135Ser
|
|
|
XM_006723733.1:c.2902G>T
|
XP_006723796.1:p.Ala968Ser
|
|
|
XM_011528647.1:c.3850G>T
|
XP_011526949.1:p.Ala1284Ser
|
|
|
XM_011528648.1:c.3847G>T
|
XP_011526950.1:p.Ala1283Ser
|
|
|
XM_011528649.1:c.3766G>T
|
XP_011526951.1:p.Ala1256Ser
|
|
|
XM_011528650.1:c.3697G>T
|
XP_011526952.1:p.Ala1233Ser
|
|
|
XM_011528651.1:c.3565G>T
|
XP_011526953.1:p.Ala1189Ser
|
|
|
XM_011528652.1:c.3502G>T
|
XP_011526954.1:p.Ala1168Ser
|
|
|
NM_001363734.1:c.3403G>T
|
NP_001350663.1:p.Ala1135Ser
|
|
|
XM_006723727.3:c.3583G>T
|
XP_006723790.1:p.Ala1195Ser
|
|
|
XM_006723728.3:c.3556G>T
|
XP_006723791.1:p.Ala1186Ser
|
|
|
XM_006723730.4:c.3502G>T
|
XP_006723793.1:p.Ala1168Ser
|
|
|
XM_011528648.3:c.3847G>T
|
XP_011526950.1:p.Ala1283Ser
|
|
|
XM_011528652.2:c.3502G>T
|
XP_011526954.1:p.Ala1168Ser
|
|
|
XM_017027704.1:c.3502G>T
|
XP_016883193.1:p.Ala1168Ser
|
|
|
XM_017027705.1:c.3502G>T
|
XP_016883194.1:p.Ala1168Ser
|
|
|
XM_017027706.1:c.3433G>T
|
XP_016883195.1:p.Ala1145Ser
|
|
|
NM_015338.6:c.3586G>T
MANE Select
|
NP_056153.2:p.Ala1196Ser
|
|
