ENST00000526209.2:c.279A>T
|
|
|
ENST00000681974.1:n.981A>T
|
|
|
ENST00000682693.1:n.1943A>T
|
|
|
ENST00000682886.1:n.479A>T
|
|
|
ENST00000683543.2:c.16357A>T
|
ENSP00000506726.1:p.Asn5453Tyr
|
|
ENST00000683988.1:c.280A>T
|
ENSP00000506939.1:p.Asn94Tyr
|
|
ENST00000684428.1:c.844A>T
|
ENSP00000507433.1:p.Asn282Tyr
|
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ENST00000684755.1:n.892A>T
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|
|
ENST00000685024.1:c.1463A>T
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|
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ENST00000685166.1:c.16318A>T
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ENSP00000509386.1:p.Asn5440Tyr
|
|
ENST00000688411.1:c.786A>T
|
ENSP00000510146.1:n.786A>T
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|
ENST00000691932.1:c.310A>T
|
ENSP00000509037.1:p.Asn104Tyr
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|
ENST00000692637.1:c.16306A>T
|
ENSP00000509666.1:p.Asn5436Tyr
|
|
ENST00000301067.12:c.16309A>T
MANE Select
|
ENSP00000301067.7:p.Asn5437Tyr
|
|
ENST00000301067.11:c.16309A>T
|
ENSP00000301067.7:p.Asn5437Tyr
|
|
ENST00000526209.1:c.352A>T
|
ENSP00000435714.1:p.Asn118Tyr
|
|
NM_003482.3:c.16309A>T
|
NP_003473.3:p.Asn5437Tyr
|
|
XM_005269162.3:c.16309A>T
|
XP_005269219.1:p.Asn5437Tyr
|
|
XM_006719614.2:c.16318A>T
|
XP_006719677.1:p.Asn5440Tyr
|
|
XM_006719616.2:c.16306A>T
|
XP_006719679.1:p.Asn5436Tyr
|
|
XM_011538770.1:c.16366A>T
|
XP_011537072.1:p.Asn5456Tyr
|
|
XM_011538771.1:c.16363A>T
|
XP_011537073.1:p.Asn5455Tyr
|
|
XM_011538772.1:c.16357A>T
|
XP_011537074.1:p.Asn5453Tyr
|
|
XM_011538773.1:c.16354A>T
|
XP_011537075.1:p.Asn5452Tyr
|
|
XM_011538774.1:c.16345A>T
|
XP_011537076.1:p.Asn5449Tyr
|
|
XM_011538775.1:c.16300A>T
|
XP_011537077.1:p.Asn5434Tyr
|
|
XM_011538776.1:c.16273A>T
|
XP_011537078.1:p.Asn5425Tyr
|
|
XM_005269162.4:c.16309A>T
|
XP_005269219.1:p.Asn5437Tyr
|
|
XM_006719614.4:c.16318A>T
|
XP_006719677.1:p.Asn5440Tyr
|
|
XM_006719616.3:c.16306A>T
|
XP_006719679.1:p.Asn5436Tyr
|
|
XM_011538770.2:c.16366A>T
|
XP_011537072.1:p.Asn5456Tyr
|
|
XM_011538771.2:c.16363A>T
|
XP_011537073.1:p.Asn5455Tyr
|
|
XM_011538772.2:c.16357A>T
|
XP_011537074.1:p.Asn5453Tyr
|
|
XM_011538773.2:c.16354A>T
|
XP_011537075.1:p.Asn5452Tyr
|
|
XM_011538774.2:c.16345A>T
|
XP_011537076.1:p.Asn5449Tyr
|
|
XM_011538776.2:c.16273A>T
|
XP_011537078.1:p.Asn5425Tyr
|
|
XR_001748874.1:n.16486A>T
|
|
|
NM_003482.4:c.16309A>T
MANE Select
|
NP_003473.3:p.Asn5437Tyr
|
|