ENST00000261769.10:c.1478T>C
MANE Select
|
ENSP00000261769.4:p.Val493Ala
|
|
ENST00000261769.9:c.1478T>C
|
ENSP00000261769.4:p.Val493Ala
|
|
ENST00000422392.6:c.1295T>C
|
ENSP00000414946.2:p.Val432Ala
|
|
ENST00000562836.5:n.1549T>C
|
|
|
ENST00000566510.5:c.*144T>C
|
ENSP00000458139.1:n.*144T>C
|
|
ENST00000566612.5:c.1478T>C
|
ENSP00000454782.1:p.Val493Ala
|
|
ENST00000611625.4:c.1541T>C
|
ENSP00000481063.1:p.Val514Ala
|
|
ENST00000612417.4:c.1478T>C
|
ENSP00000478360.1:p.Val493Ala
|
|
ENST00000621016.4:c.1478T>C
|
ENSP00000480664.1:p.Val493Ala
|
|
NM_004360.3:c.1478T>C , LRG_301t1:c.1478T>C
|
NP_004351.1:p.Val493Ala
|
|
XM_011523488.1:c.743T>C
|
XP_011521790.1:p.Val248Ala
|
|
XM_011523489.1:c.743T>C
|
XP_011521791.1:p.Val248Ala
|
|
NM_001317184.1:c.1295T>C
|
NP_001304113.1:p.Val432Ala
|
|
NM_001317185.1:c.-71T>C
|
NP_001304114.1:n.-71T>C
|
|
NM_001317186.1:c.-342T>C
|
NP_001304115.1:n.-342T>C
|
|
NM_004360.4:c.1478T>C
|
NP_004351.1:p.Val493Ala
|
|
NM_004360.5:c.1478T>C
MANE Select
|
NP_004351.1:p.Val493Ala
|
|
NM_001317184.2:c.1295T>C
|
NP_001304113.1:p.Val432Ala
|
|
NM_001317185.2:c.-71T>C
|
NP_001304114.1:n.-71T>C
|
|
NM_001317186.2:c.-342T>C
|
NP_001304115.1:n.-342T>C
|
|