ENST00000526209.2:c.298A>C
|
|
|
ENST00000681974.1:n.1000A>C
|
|
|
ENST00000682693.1:n.1962A>C
|
|
|
ENST00000682886.1:n.498A>C
|
|
|
ENST00000683543.2:c.16376A>C
|
ENSP00000506726.1:p.Tyr5459Ser
|
|
ENST00000683988.1:c.299A>C
|
ENSP00000506939.1:p.Tyr100Ser
|
|
ENST00000684428.1:c.863A>C
|
ENSP00000507433.1:p.Tyr288Ser
|
|
ENST00000684755.1:n.911A>C
|
|
|
ENST00000685024.1:c.1482A>C
|
|
|
ENST00000685166.1:c.16337A>C
|
ENSP00000509386.1:p.Tyr5446Ser
|
|
ENST00000688411.1:c.805A>C
|
ENSP00000510146.1:n.805A>C
|
|
ENST00000691932.1:c.329A>C
|
ENSP00000509037.1:p.Tyr110Ser
|
|
ENST00000692637.1:c.16325A>C
|
ENSP00000509666.1:p.Tyr5442Ser
|
|
ENST00000301067.12:c.16328A>C
MANE Select
|
ENSP00000301067.7:p.Tyr5443Ser
|
|
ENST00000301067.11:c.16328A>C
|
ENSP00000301067.7:p.Tyr5443Ser
|
|
ENST00000526209.1:c.371A>C
|
ENSP00000435714.1:p.Tyr124Ser
|
|
NM_003482.3:c.16328A>C
|
NP_003473.3:p.Tyr5443Ser
|
|
XM_005269162.3:c.16328A>C
|
XP_005269219.1:p.Tyr5443Ser
|
|
XM_006719614.2:c.16337A>C
|
XP_006719677.1:p.Tyr5446Ser
|
|
XM_006719616.2:c.16325A>C
|
XP_006719679.1:p.Tyr5442Ser
|
|
XM_011538770.1:c.16385A>C
|
XP_011537072.1:p.Tyr5462Ser
|
|
XM_011538771.1:c.16382A>C
|
XP_011537073.1:p.Tyr5461Ser
|
|
XM_011538772.1:c.16376A>C
|
XP_011537074.1:p.Tyr5459Ser
|
|
XM_011538773.1:c.16373A>C
|
XP_011537075.1:p.Tyr5458Ser
|
|
XM_011538774.1:c.16364A>C
|
XP_011537076.1:p.Tyr5455Ser
|
|
XM_011538775.1:c.16319A>C
|
XP_011537077.1:p.Tyr5440Ser
|
|
XM_011538776.1:c.16292A>C
|
XP_011537078.1:p.Tyr5431Ser
|
|
XM_005269162.4:c.16328A>C
|
XP_005269219.1:p.Tyr5443Ser
|
|
XM_006719614.4:c.16337A>C
|
XP_006719677.1:p.Tyr5446Ser
|
|
XM_006719616.3:c.16325A>C
|
XP_006719679.1:p.Tyr5442Ser
|
|
XM_011538770.2:c.16385A>C
|
XP_011537072.1:p.Tyr5462Ser
|
|
XM_011538771.2:c.16382A>C
|
XP_011537073.1:p.Tyr5461Ser
|
|
XM_011538772.2:c.16376A>C
|
XP_011537074.1:p.Tyr5459Ser
|
|
XM_011538773.2:c.16373A>C
|
XP_011537075.1:p.Tyr5458Ser
|
|
XM_011538774.2:c.16364A>C
|
XP_011537076.1:p.Tyr5455Ser
|
|
XM_011538776.2:c.16292A>C
|
XP_011537078.1:p.Tyr5431Ser
|
|
XR_001748874.1:n.16505A>C
|
|
|
NM_003482.4:c.16328A>C
MANE Select
|
NP_003473.3:p.Tyr5443Ser
|
|