ENST00000029410.10:c.189A>T
MANE Select
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ENSP00000029410.5:p.Gly63=
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ENST00000029410.9:c.189A>T
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ENSP00000029410.5:p.Gly63=
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ENST00000502420.1:n.168A>T
|
|
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ENST00000505433.5:c.189A>T
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ENSP00000425591.1:p.Gly63=
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|
ENST00000505468.1:c.-154A>T
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ENSP00000420886.1:n.-154A>T
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ENST00000507061.1:c.6A>T
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ENSP00000423868.1:p.Gly2=
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ENST00000510761.1:c.-154A>T
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ENSP00000423438.1:n.-154A>T
|
|
NM_007255.2:c.189A>T
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NP_009186.1:p.Gly63=
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|
XM_005265805.2:c.-154A>T
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XP_005265862.1:n.-154A>T
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XM_006714816.2:c.-311A>T
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XP_006714879.1:n.-311A>T
|
|
XM_011534421.1:c.-154A>T
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XP_011532723.1:n.-154A>T
|
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XM_006714816.4:c.-311A>T
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XP_006714879.1:n.-311A>T
|
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XM_017008999.2:c.-154A>T
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XP_016864488.1:n.-154A>T
|
|
NM_007255.3:c.189A>T
MANE Select
|
NP_009186.1:p.Gly63=
|
|