|
ENST00000336592.11:c.1802G>T
|
ENSP00000338919.6:p.Arg601Leu
|
|
|
ENST00000371322.11:c.1787G>T
MANE Select
|
ENSP00000360373.5:p.Arg596Leu
|
|
|
ENST00000371323.3:c.1253G>T
|
ENSP00000360374.3:p.Arg418Leu
|
|
|
ENST00000404115.8:c.1787G>T
|
ENSP00000384109.4:p.Arg596Leu
|
|
|
ENST00000673919.1:c.*1234G>T
|
ENSP00000500994.1:n.*1234G>T
|
|
|
ENST00000674073.2:c.1231G>T
|
|
|
|
ENST00000674137.11:c.1787G>T
|
ENSP00000501019.6:p.Arg596Leu
|
|
|
ENST00000679405.1:c.*996G>T
|
ENSP00000504985.1:n.*996G>T
|
|
|
ENST00000679432.1:c.1892G>T
|
|
|
|
ENST00000679844.1:c.1126G>T
|
|
|
|
ENST00000679927.1:c.1442G>T
|
ENSP00000505603.1:p.Arg481Leu
|
|
|
ENST00000679965.1:n.367G>T
|
|
|
|
ENST00000680165.1:n.2113G>T
|
|
|
|
ENST00000680324.1:n.3195G>T
|
|
|
|
ENST00000680457.1:n.1215G>T
|
|
|
|
ENST00000680474.1:c.1231G>T
|
|
|
|
ENST00000680577.1:n.1948G>T
|
|
|
|
ENST00000680673.1:c.1841G>T
|
ENSP00000505084.1:p.Arg614Leu
|
|
|
ENST00000680918.1:c.1068G>T
|
|
|
|
ENST00000681080.1:c.1277G>T
|
|
|
|
ENST00000681090.1:c.1694G>T
|
ENSP00000506288.1:p.Arg565Leu
|
|
|
ENST00000681189.1:c.1231G>T
|
|
|
|
ENST00000681206.1:c.1901G>T
|
ENSP00000505480.1:p.Arg634Leu
|
|
|
ENST00000681253.1:c.1841G>T
|
ENSP00000506259.1:p.Arg614Leu
|
|
|
ENST00000681263.1:n.181G>T
|
|
|
|
ENST00000681333.1:c.*2230G>T
|
ENSP00000505739.1:n.*2230G>T
|
|
|
ENST00000681652.1:c.1841G>T
|
ENSP00000505176.1:p.Arg614Leu
|
|
|
ENST00000681864.1:n.3925G>T
|
|
|
|
ENST00000681869.1:c.1231G>T
|
|
|
|
ENST00000681908.1:c.1231G>T
|
|
|
|
ENST00000336592.10:c.1802G>T
|
ENSP00000338919.6:p.Arg601Leu
|
|
|
ENST00000371322.9:c.1787G>T
|
ENSP00000360373.5:p.Arg596Leu
|
|
|
ENST00000404115.7:c.1841G>T
|
ENSP00000384109.3:p.Arg614Leu
|
|
|
NM_001079872.1:c.1787G>T
|
NP_001073341.1:p.Arg596Leu
|
|
|
NM_003588.3:c.1841G>T
|
NP_003579.3:p.Arg614Leu
|
|
|
XM_005262481.1:c.1841G>T
|
XP_005262538.1:p.Arg614Leu
|
|
|
XM_006724784.1:c.1802G>T
|
XP_006724847.1:p.Arg601Leu
|
|
|
XM_006724785.1:c.1802G>T
|
XP_006724848.1:p.Arg601Leu
|
|
|
XM_011531399.1:c.1253G>T
|
XP_011529701.1:p.Arg418Leu
|
|
|
XM_011531400.1:c.1253G>T
|
XP_011529702.1:p.Arg418Leu
|
|
|
XM_011531401.1:c.1199G>T
|
XP_011529703.1:p.Arg400Leu
|
|
|
NM_001330624.1:c.1802G>T
|
NP_001317553.1:p.Arg601Leu
|
|
|
XM_011531399.2:c.1253G>T
|
XP_011529701.1:p.Arg418Leu
|
|
|
XM_011531400.2:c.1253G>T
|
XP_011529702.1:p.Arg418Leu
|
|
|
NM_001079872.2:c.1787G>T
MANE Select
|
NP_001073341.1:p.Arg596Leu
|
|
|
NM_001369145.1:c.1253G>T
|
NP_001356074.1:p.Arg418Leu
|
|
|
NM_001330624.2:c.1802G>T
|
NP_001317553.1:p.Arg601Leu
|
|
|
NM_003588.4:c.1841G>T
|
NP_003579.3:p.Arg614Leu
|
|
