ENST00000262494.13:c.626G>A
|
ENSP00000262494.7:p.Arg209His
|
|
ENST00000262493.12:c.626G>A
MANE Select
|
ENSP00000262493.6:p.Arg209His
|
|
ENST00000262494.12:c.626G>A
|
ENSP00000262494.7:p.Arg209His
|
|
ENST00000562316.6:c.293G>A
|
ENSP00000457238.2:p.Arg98His
|
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ENST00000568375.2:c.18G>A
|
|
|
ENST00000638185.1:n.841G>A
|
|
|
ENST00000638210.1:n.926G>A
|
|
|
ENST00000638705.1:c.626G>A
|
ENSP00000491223.1:p.Arg209His
|
|
ENST00000638836.1:n.536G>A
|
|
|
ENST00000639055.1:n.1347G>A
|
|
|
ENST00000639251.1:n.527G>A
|
|
|
ENST00000639268.1:c.261G>A
|
|
|
ENST00000639341.1:c.151G>A
|
|
|
ENST00000639770.1:c.664G>A
|
ENSP00000491999.1:n.664G>A
|
|
ENST00000640390.1:n.556G>A
|
|
|
ENST00000640560.1:n.402G>A
|
|
|
ENST00000640893.1:c.*24G>A
|
ENSP00000492677.1:n.*24G>A
|
|
ENST00000262493.10:c.626G>A
|
ENSP00000262493.6:p.Arg209His
|
|
ENST00000262494.11:c.626G>A
|
ENSP00000262494.7:p.Arg209His
|
|
ENST00000568375.1:n.18G>A
|
|
|
NM_020988.2:c.626G>A
|
NP_066268.1:p.Arg209His
|
|
NM_138736.2:c.626G>A
|
NP_620073.2:p.Arg209His
|
|
XM_011523003.1:c.500G>A
|
XP_011521305.1:p.Arg167His
|
|
XM_011523003.3:c.500G>A
|
XP_011521305.1:p.Arg167His
|
|
NM_020988.3:c.626G>A
MANE Select
|
NP_066268.1:p.Arg209His
|
|
NM_138736.3:c.626G>A
|
NP_620073.2:p.Arg209His
|
|