ENST00000326735.13:c.3513G>A
MANE Select
|
ENSP00000327214.8:p.Trp1171Ter
|
|
ENST00000326735.12:c.3513G>A
|
ENSP00000327214.8:p.Trp1171Ter
|
|
ENST00000341676.9:c.3211G>A
|
ENSP00000341115.5:p.Ala1071Thr
|
|
ENST00000452699.5:c.3498G>A
|
ENSP00000413307.1:p.Trp1166Ter
|
|
ENST00000466561.1:n.1559G>A
|
|
|
ENST00000502418.1:c.931G>A
|
ENSP00000423065.1:p.Ala311Thr
|
|
NM_001141973.2:c.3498G>A
|
NP_001135445.1:p.Trp1166Ter
|
|
NM_001141974.2:c.3211G>A
|
NP_001135446.1:p.Ala1071Thr
|
|
NM_022089.3:c.3513G>A
|
NP_071372.1:p.Trp1171Ter
|
|
XM_005245809.1:c.3343G>A
|
XP_005245866.1:p.Ala1115Thr
|
|
XM_005245810.1:c.3340G>A
|
XP_005245867.1:p.Ala1114Thr
|
|
XM_005245811.1:c.3328G>A
|
XP_005245868.1:p.Ala1110Thr
|
|
XM_005245812.1:c.3316G>A
|
XP_005245869.1:p.Ala1106Thr
|
|
XM_005245813.1:c.3283G>A
|
XP_005245870.1:p.Ala1095Thr
|
|
XM_005245815.1:c.3226G>A
|
XP_005245872.1:p.Ala1076Thr
|
|
XM_006710512.1:c.3325G>A
|
XP_006710575.1:p.Ala1109Thr
|
|
XM_006710513.1:c.3301G>A
|
XP_006710576.1:p.Ala1101Thr
|
|
XM_011541128.1:c.3328G>A
|
XP_011539430.1:p.Ala1110Thr
|
|
XM_011541129.1:c.3136G>A
|
XP_011539431.1:p.Ala1046Thr
|
|
XM_017000844.1:c.3498G>A
|
XP_016856333.1:p.Trp1166Ter
|
|
XM_017000845.1:c.3495G>A
|
XP_016856334.1:p.Trp1165Ter
|
|
XM_017000846.1:c.3471G>A
|
XP_016856335.1:p.Trp1157Ter
|
|
XM_017000847.1:c.3468G>A
|
XP_016856336.1:p.Trp1156Ter
|
|
XM_017000848.1:c.3396G>A
|
XP_016856337.1:p.Trp1132Ter
|
|
XM_017000849.1:c.3381G>A
|
XP_016856338.1:p.Trp1127Ter
|
|
XM_017000850.1:c.3306G>A
|
XP_016856339.1:p.Trp1102Ter
|
|
NM_022089.4:c.3513G>A
MANE Select
|
NP_071372.1:p.Trp1171Ter
|
|
NM_001141973.3:c.3498G>A
|
NP_001135445.1:p.Trp1166Ter
|
|
NM_001141974.3:c.3211G>A
|
NP_001135446.1:p.Ala1071Thr
|
|