ENST00000526209.2:c.298A>T
|
|
|
ENST00000681974.1:n.1000A>T
|
|
|
ENST00000682693.1:n.1962A>T
|
|
|
ENST00000682886.1:n.498A>T
|
|
|
ENST00000683543.2:c.16376A>T
|
ENSP00000506726.1:p.Tyr5459Phe
|
|
ENST00000683988.1:c.299A>T
|
ENSP00000506939.1:p.Tyr100Phe
|
|
ENST00000684428.1:c.863A>T
|
ENSP00000507433.1:p.Tyr288Phe
|
|
ENST00000684755.1:n.911A>T
|
|
|
ENST00000685024.1:c.1482A>T
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|
|
ENST00000685166.1:c.16337A>T
|
ENSP00000509386.1:p.Tyr5446Phe
|
|
ENST00000688411.1:c.805A>T
|
ENSP00000510146.1:n.805A>T
|
|
ENST00000691932.1:c.329A>T
|
ENSP00000509037.1:p.Tyr110Phe
|
|
ENST00000692637.1:c.16325A>T
|
ENSP00000509666.1:p.Tyr5442Phe
|
|
ENST00000301067.12:c.16328A>T
MANE Select
|
ENSP00000301067.7:p.Tyr5443Phe
|
|
ENST00000301067.11:c.16328A>T
|
ENSP00000301067.7:p.Tyr5443Phe
|
|
ENST00000526209.1:c.371A>T
|
ENSP00000435714.1:p.Tyr124Phe
|
|
NM_003482.3:c.16328A>T
|
NP_003473.3:p.Tyr5443Phe
|
|
XM_005269162.3:c.16328A>T
|
XP_005269219.1:p.Tyr5443Phe
|
|
XM_006719614.2:c.16337A>T
|
XP_006719677.1:p.Tyr5446Phe
|
|
XM_006719616.2:c.16325A>T
|
XP_006719679.1:p.Tyr5442Phe
|
|
XM_011538770.1:c.16385A>T
|
XP_011537072.1:p.Tyr5462Phe
|
|
XM_011538771.1:c.16382A>T
|
XP_011537073.1:p.Tyr5461Phe
|
|
XM_011538772.1:c.16376A>T
|
XP_011537074.1:p.Tyr5459Phe
|
|
XM_011538773.1:c.16373A>T
|
XP_011537075.1:p.Tyr5458Phe
|
|
XM_011538774.1:c.16364A>T
|
XP_011537076.1:p.Tyr5455Phe
|
|
XM_011538775.1:c.16319A>T
|
XP_011537077.1:p.Tyr5440Phe
|
|
XM_011538776.1:c.16292A>T
|
XP_011537078.1:p.Tyr5431Phe
|
|
XM_005269162.4:c.16328A>T
|
XP_005269219.1:p.Tyr5443Phe
|
|
XM_006719614.4:c.16337A>T
|
XP_006719677.1:p.Tyr5446Phe
|
|
XM_006719616.3:c.16325A>T
|
XP_006719679.1:p.Tyr5442Phe
|
|
XM_011538770.2:c.16385A>T
|
XP_011537072.1:p.Tyr5462Phe
|
|
XM_011538771.2:c.16382A>T
|
XP_011537073.1:p.Tyr5461Phe
|
|
XM_011538772.2:c.16376A>T
|
XP_011537074.1:p.Tyr5459Phe
|
|
XM_011538773.2:c.16373A>T
|
XP_011537075.1:p.Tyr5458Phe
|
|
XM_011538774.2:c.16364A>T
|
XP_011537076.1:p.Tyr5455Phe
|
|
XM_011538776.2:c.16292A>T
|
XP_011537078.1:p.Tyr5431Phe
|
|
XR_001748874.1:n.16505A>T
|
|
|
NM_003482.4:c.16328A>T
MANE Select
|
NP_003473.3:p.Tyr5443Phe
|
|