ENST00000223051.8:c.2036G>C
MANE Select
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ENSP00000223051.3:p.Gly679Ala
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ENST00000223051.7:c.2036G>C
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ENSP00000223051.3:p.Gly679Ala
|
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ENST00000431692.5:c.*711G>C
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ENSP00000413905.1:n.*711G>C
|
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ENST00000461176.1:n.382G>C
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|
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ENST00000462090.5:n.1072G>C
|
|
|
ENST00000462107.1:c.2036G>C
|
ENSP00000420525.1:p.Gly679Ala
|
|
ENST00000465294.5:n.1956G>C
|
|
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ENST00000476304.5:n.1657G>C
|
|
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ENST00000490084.5:c.1389G>C
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|
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NM_001206855.1:c.1523G>C
|
NP_001193784.1:p.Gly508Ala
|
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NM_003227.3:c.2036G>C
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NP_003218.2:p.Gly679Ala
|
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XM_005250553.3:c.2036G>C
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XP_005250610.1:p.Gly679Ala
|
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XM_005250554.3:c.2036G>C
|
XP_005250611.1:p.Gly679Ala
|
|
XR_927814.1:n.434-4293C>G
|
|
|
NM_001206855.2:c.1523G>C
|
NP_001193784.1:p.Gly508Ala
|
|
XM_005250553.4:c.2036G>C
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XP_005250610.1:p.Gly679Ala
|
|
XM_017012573.1:c.2036G>C
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XP_016868062.1:p.Gly679Ala
|
|
NM_003227.4:c.2036G>C
MANE Select
|
NP_003218.2:p.Gly679Ala
|
|
NM_001206855.3:c.1523G>C
|
NP_001193784.1:p.Gly508Ala
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