ENST00000261937.11:c.3793T>C
MANE Select
|
ENSP00000261937.6:p.Tyr1265His
|
|
ENST00000261937.10:c.3793T>C
|
ENSP00000261937.6:p.Tyr1265His
|
|
ENST00000393347.7:c.3793T>C
|
ENSP00000377016.3:p.Tyr1265His
|
|
ENST00000502603.5:n.493T>C
|
|
|
ENST00000502649.5:c.3793T>C
|
ENSP00000426057.1:p.Tyr1265His
|
|
ENST00000507059.5:n.4143T>C
|
|
|
ENST00000619105.4:c.*2736T>C
|
ENSP00000481134.1:n.*2736T>C
|
|
NM_002020.4:c.3793T>C
|
NP_002011.2:p.Tyr1265His
|
|
NM_182925.4:c.3793T>C
|
NP_891555.2:p.Tyr1265His
|
|
XM_011534477.1:c.4042T>C
|
XP_011532779.1:p.Tyr1348His
|
|
XM_011534478.1:c.4024T>C
|
XP_011532780.1:p.Tyr1342His
|
|
XM_011534479.1:c.4042T>C
|
XP_011532781.1:p.Tyr1348His
|
|
XM_011534480.1:c.4042T>C
|
XP_011532782.1:p.Tyr1348His
|
|
XM_011534481.1:c.4042T>C
|
XP_011532783.1:p.Tyr1348His
|
|
XM_011534482.1:c.3811T>C
|
XP_011532784.1:p.Tyr1271His
|
|
XM_011534483.1:c.3733T>C
|
XP_011532785.1:p.Tyr1245His
|
|
XM_011534484.1:c.3334T>C
|
XP_011532786.1:p.Tyr1112His
|
|
XR_941095.1:n.4079T>C
|
|
|
NM_001354989.1:c.3793T>C
|
NP_001341918.1:p.Tyr1265His
|
|
XM_011534478.3:c.4024T>C
|
XP_011532780.1:p.Tyr1342His
|
|
XM_011534484.2:c.3334T>C
|
XP_011532786.1:p.Tyr1112His
|
|
XM_017009263.1:c.4024T>C
|
XP_016864752.1:p.Tyr1342His
|
|
XM_017009264.2:c.4024T>C
|
XP_016864753.1:p.Tyr1342His
|
|
XM_017009265.1:c.4024T>C
|
XP_016864754.1:p.Tyr1342His
|
|
XM_017009266.1:c.4024T>C
|
XP_016864755.1:p.Tyr1342His
|
|
XM_017009267.2:c.4024T>C
|
XP_016864756.1:p.Tyr1342His
|
|
XM_017009268.1:c.3715T>C
|
XP_016864757.1:p.Tyr1239His
|
|
XR_001742050.2:n.4283T>C
|
|
|
NM_182925.5:c.3793T>C
MANE Select
|
NP_891555.2:p.Tyr1265His
|
|
NM_001354989.2:c.3793T>C
|
NP_001341918.1:p.Tyr1265His
|
|
NM_002020.5:c.3793T>C
|
NP_002011.2:p.Tyr1265His
|
|