|
ENST00000336592.11:c.1675C>T
|
ENSP00000338919.6:p.Arg559Cys
|
|
|
ENST00000371322.11:c.1660C>T
MANE Select
|
ENSP00000360373.5:p.Arg554Cys
|
|
|
ENST00000371323.3:c.1126C>T
|
ENSP00000360374.3:p.Arg376Cys
|
|
|
ENST00000404115.8:c.1660C>T
|
ENSP00000384109.4:p.Arg554Cys
|
|
|
ENST00000673919.1:c.*1107C>T
|
ENSP00000500994.1:n.*1107C>T
|
|
|
ENST00000674073.2:c.1104C>T
|
|
|
|
ENST00000674137.11:c.1660C>T
|
ENSP00000501019.6:p.Arg554Cys
|
|
|
ENST00000679405.1:c.*869C>T
|
ENSP00000504985.1:n.*869C>T
|
|
|
ENST00000679432.1:c.1765C>T
|
|
|
|
ENST00000679844.1:c.1081-579C>T
|
|
|
|
ENST00000679927.1:c.1315C>T
|
ENSP00000505603.1:p.Arg439Cys
|
|
|
ENST00000679965.1:n.240C>T
|
|
|
|
ENST00000680165.1:n.1986C>T
|
|
|
|
ENST00000680324.1:n.2571C>T
|
|
|
|
ENST00000680457.1:n.1088C>T
|
|
|
|
ENST00000680474.1:c.1104C>T
|
|
|
|
ENST00000680577.1:n.1821C>T
|
|
|
|
ENST00000680673.1:c.1714C>T
|
ENSP00000505084.1:p.Arg572Cys
|
|
|
ENST00000680918.1:c.941C>T
|
|
|
|
ENST00000681080.1:c.1150C>T
|
|
|
|
ENST00000681090.1:c.1567C>T
|
ENSP00000506288.1:p.Arg523Cys
|
|
|
ENST00000681189.1:c.1104C>T
|
|
|
|
ENST00000681206.1:c.1774C>T
|
ENSP00000505480.1:p.Arg592Cys
|
|
|
ENST00000681253.1:c.1714C>T
|
ENSP00000506259.1:p.Arg572Cys
|
|
|
ENST00000681263.1:n.54C>T
|
|
|
|
ENST00000681333.1:c.*1606C>T
|
ENSP00000505739.1:n.*1606C>T
|
|
|
ENST00000681652.1:c.1714C>T
|
ENSP00000505176.1:p.Arg572Cys
|
|
|
ENST00000681864.1:n.3301C>T
|
|
|
|
ENST00000681869.1:c.1104C>T
|
|
|
|
ENST00000681908.1:c.1104C>T
|
|
|
|
ENST00000336592.10:c.1675C>T
|
ENSP00000338919.6:p.Arg559Cys
|
|
|
ENST00000371322.9:c.1660C>T
|
ENSP00000360373.5:p.Arg554Cys
|
|
|
ENST00000404115.7:c.1714C>T
|
ENSP00000384109.3:p.Arg572Cys
|
|
|
NM_001079872.1:c.1660C>T
|
NP_001073341.1:p.Arg554Cys
|
|
|
NM_003588.3:c.1714C>T
|
NP_003579.3:p.Arg572Cys
|
|
|
XM_005262481.1:c.1714C>T
|
XP_005262538.1:p.Arg572Cys
|
|
|
XM_006724784.1:c.1675C>T
|
XP_006724847.1:p.Arg559Cys
|
|
|
XM_006724785.1:c.1675C>T
|
XP_006724848.1:p.Arg559Cys
|
|
|
XM_011531399.1:c.1126C>T
|
XP_011529701.1:p.Arg376Cys
|
|
|
XM_011531400.1:c.1126C>T
|
XP_011529702.1:p.Arg376Cys
|
|
|
XM_011531401.1:c.1072C>T
|
XP_011529703.1:p.Arg358Cys
|
|
|
NM_001330624.1:c.1675C>T
|
NP_001317553.1:p.Arg559Cys
|
|
|
XM_011531399.2:c.1126C>T
|
XP_011529701.1:p.Arg376Cys
|
|
|
XM_011531400.2:c.1126C>T
|
XP_011529702.1:p.Arg376Cys
|
|
|
NM_001079872.2:c.1660C>T
MANE Select
|
NP_001073341.1:p.Arg554Cys
|
|
|
NM_001369145.1:c.1126C>T
|
NP_001356074.1:p.Arg376Cys
|
|
|
NM_001330624.2:c.1675C>T
|
NP_001317553.1:p.Arg559Cys
|
|
|
NM_003588.4:c.1714C>T
|
NP_003579.3:p.Arg572Cys
|
|
