ENST00000526209.2:c.402G>T
|
|
|
ENST00000681974.1:n.1104G>T
|
|
|
ENST00000682693.1:n.2066G>T
|
|
|
ENST00000682886.1:n.838G>T
|
|
|
ENST00000683543.2:c.16480G>T
|
ENSP00000506726.1:p.Ala5494Ser
|
|
ENST00000683988.1:c.403G>T
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ENSP00000506939.1:p.Ala135Ser
|
|
ENST00000684428.1:c.1025G>T
|
ENSP00000507433.1:n.1025G>T
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|
ENST00000685024.1:c.1586G>T
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|
|
ENST00000685166.1:c.16441G>T
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ENSP00000509386.1:p.Ala5481Ser
|
|
ENST00000691932.1:c.433G>T
|
ENSP00000509037.1:p.Ala145Ser
|
|
ENST00000692637.1:c.16429G>T
|
ENSP00000509666.1:p.Ala5477Ser
|
|
ENST00000301067.12:c.16432G>T
MANE Select
|
ENSP00000301067.7:p.Ala5478Ser
|
|
ENST00000301067.11:c.16432G>T
|
ENSP00000301067.7:p.Ala5478Ser
|
|
ENST00000526209.1:c.475G>T
|
ENSP00000435714.1:p.Ala159Ser
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|
NM_003482.3:c.16432G>T
|
NP_003473.3:p.Ala5478Ser
|
|
XM_005269162.3:c.16432G>T
|
XP_005269219.1:p.Ala5478Ser
|
|
XM_006719614.2:c.16441G>T
|
XP_006719677.1:p.Ala5481Ser
|
|
XM_006719616.2:c.16429G>T
|
XP_006719679.1:p.Ala5477Ser
|
|
XM_011538770.1:c.16489G>T
|
XP_011537072.1:p.Ala5497Ser
|
|
XM_011538771.1:c.16486G>T
|
XP_011537073.1:p.Ala5496Ser
|
|
XM_011538772.1:c.16480G>T
|
XP_011537074.1:p.Ala5494Ser
|
|
XM_011538773.1:c.16477G>T
|
XP_011537075.1:p.Ala5493Ser
|
|
XM_011538774.1:c.16468G>T
|
XP_011537076.1:p.Ala5490Ser
|
|
XM_011538775.1:c.16423G>T
|
XP_011537077.1:p.Ala5475Ser
|
|
XM_011538776.1:c.16396G>T
|
XP_011537078.1:p.Ala5466Ser
|
|
XM_005269162.4:c.16432G>T
|
XP_005269219.1:p.Ala5478Ser
|
|
XM_006719614.4:c.16441G>T
|
XP_006719677.1:p.Ala5481Ser
|
|
XM_006719616.3:c.16429G>T
|
XP_006719679.1:p.Ala5477Ser
|
|
XM_011538770.2:c.16489G>T
|
XP_011537072.1:p.Ala5497Ser
|
|
XM_011538771.2:c.16486G>T
|
XP_011537073.1:p.Ala5496Ser
|
|
XM_011538772.2:c.16480G>T
|
XP_011537074.1:p.Ala5494Ser
|
|
XM_011538773.2:c.16477G>T
|
XP_011537075.1:p.Ala5493Ser
|
|
XM_011538774.2:c.16468G>T
|
XP_011537076.1:p.Ala5490Ser
|
|
XM_011538776.2:c.16396G>T
|
XP_011537078.1:p.Ala5466Ser
|
|
XR_001748874.1:n.16609G>T
|
|
|
NM_003482.4:c.16432G>T
MANE Select
|
NP_003473.3:p.Ala5478Ser
|
|