ENST00000029410.10:c.187G>T
MANE Select
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ENSP00000029410.5:p.Gly63Ter
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ENST00000029410.9:c.187G>T
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ENSP00000029410.5:p.Gly63Ter
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ENST00000502420.1:n.166G>T
|
|
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ENST00000505433.5:c.187G>T
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ENSP00000425591.1:p.Gly63Ter
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ENST00000505468.1:c.-156G>T
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ENSP00000420886.1:n.-156G>T
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ENST00000507061.1:c.4G>T
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ENSP00000423868.1:p.Gly2Ter
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ENST00000510761.1:c.-156G>T
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ENSP00000423438.1:n.-156G>T
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NM_007255.2:c.187G>T
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NP_009186.1:p.Gly63Ter
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XM_005265805.2:c.-156G>T
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XP_005265862.1:n.-156G>T
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XM_006714816.2:c.-313G>T
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XP_006714879.1:n.-313G>T
|
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XM_011534421.1:c.-156G>T
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XP_011532723.1:n.-156G>T
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XM_006714816.4:c.-313G>T
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XP_006714879.1:n.-313G>T
|
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XM_017008999.2:c.-156G>T
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XP_016864488.1:n.-156G>T
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NM_007255.3:c.187G>T
MANE Select
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NP_009186.1:p.Gly63Ter
|
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