ENST00000262493.12:c.974G>T
MANE Select
|
ENSP00000262493.6:p.Cys325Phe
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ENST00000562316.6:c.545-1141G>T
|
ENSP00000457238.2:n.545-1141G>T
|
|
ENST00000564727.2:c.278G>T
|
ENSP00000454971.2:p.Cys93Phe
|
|
ENST00000568375.2:c.212G>T
|
|
|
ENST00000638210.1:n.1274G>T
|
|
|
ENST00000638705.1:c.974G>T
|
ENSP00000491223.1:p.Cys325Phe
|
|
ENST00000638836.1:n.884G>T
|
|
|
ENST00000639251.1:n.875G>T
|
|
|
ENST00000639268.1:c.609G>T
|
|
|
ENST00000639341.1:c.499G>T
|
|
|
ENST00000639770.1:c.1012G>T
|
ENSP00000491999.1:n.1012G>T
|
|
ENST00000640390.1:n.904G>T
|
|
|
ENST00000640469.1:c.338G>T
|
ENSP00000491875.1:p.Cys113Phe
|
|
ENST00000640560.1:n.750G>T
|
|
|
ENST00000640893.1:c.*372G>T
|
ENSP00000492677.1:n.*372G>T
|
|
ENST00000262493.10:c.974G>T
|
ENSP00000262493.6:p.Cys325Phe
|
|
ENST00000564727.1:c.194G>T
|
ENSP00000454971.1:p.Cys65Phe
|
|
ENST00000568375.1:n.212G>T
|
|
|
NM_020988.2:c.974G>T
|
NP_066268.1:p.Cys325Phe
|
|
XM_011523003.1:c.848G>T
|
XP_011521305.1:p.Cys283Phe
|
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XM_011523003.3:c.848G>T
|
XP_011521305.1:p.Cys283Phe
|
|
NM_020988.3:c.974G>T
MANE Select
|
NP_066268.1:p.Cys325Phe
|
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