|
NM_004360.5:c.1849G>A
MANE Select
|
NP_004351.1:p.Ala617Thr
|
|
ENST00000261769.10:c.1849G>A
MANE Select
|
ENSP00000261769.4:p.Ala617Thr
|
|
NM_001317184.1:c.1666G>A
|
NP_001304113.1:p.Ala556Thr
|
|
NM_001317184.2:c.1666G>A
|
NP_001304113.1:p.Ala556Thr
|
|
NM_001317185.1:c.301G>A
|
NP_001304114.1:p.Ala101Thr
|
|
NM_001317185.2:c.301G>A
|
NP_001304114.1:p.Ala101Thr
|
|
NM_001317186.1:c.-117G>A
|
NP_001304115.1:n.-117G>A
|
|
NM_001317186.2:c.-117G>A
|
NP_001304115.1:n.-117G>A
|
|
NM_004360.3:c.1849G>A , LRG_301t1:c.1849G>A
|
NP_004351.1:p.Ala617Thr
|
|
NM_004360.4:c.1849G>A
|
NP_004351.1:p.Ala617Thr
|
|
ENST00000261769.9:c.1849G>A
|
ENSP00000261769.4:p.Ala617Thr
|
|
ENST00000422392.6:c.1666G>A
|
ENSP00000414946.2:p.Ala556Thr
|
|
ENST00000562836.5:n.1920G>A
|
|
|
ENST00000566510.5:c.*515G>A
|
ENSP00000458139.1:n.*515G>A
|
|
ENST00000566612.5:c.*89G>A
|
ENSP00000454782.1:n.*89G>A
|
|
ENST00000611625.4:c.1912G>A
|
ENSP00000481063.1:p.Ala638Thr
|
|
ENST00000612417.4:c.1830+19G>A
|
ENSP00000478360.1:n.1830+19G>A
|
|
ENST00000621016.4:c.1849G>A
|
ENSP00000480664.1:p.Ala617Thr
|
|
XM_011523488.1:c.1114G>A
|
XP_011521790.1:p.Ala372Thr
|
|
XM_011523489.1:c.1114G>A
|
XP_011521791.1:p.Ala372Thr
|
