ENST00000368373.8:c.735C>A
MANE Select
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ENSP00000357357.3:p.His245Gln
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ENST00000327247.9:c.735C>A
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ENSP00000314508.5:p.His245Gln
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ENST00000368373.7:c.735C>A
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ENSP00000357357.3:p.His245Gln
|
|
ENST00000427500.7:c.588C>A
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ENSP00000402577.2:p.His196Gln
|
|
ENST00000428024.3:c.474C>A
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ENSP00000397986.2:p.His158Gln
|
|
ENST00000460156.1:n.522C>A
|
|
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ENST00000484489.5:n.339+1813C>A
|
|
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ENST00000491081.5:n.340C>A
|
|
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ENST00000497670.5:n.358C>A
|
|
|
NM_000157.3:c.735C>A
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NP_000148.2:p.His245Gln
|
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NM_001005741.2:c.735C>A
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NP_001005741.1:p.His245Gln
|
|
NM_001005742.2:c.735C>A
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NP_001005742.1:p.His245Gln
|
|
NM_001171811.1:c.474C>A
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NP_001165282.1:p.His158Gln
|
|
NM_001171812.1:c.588C>A
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NP_001165283.1:p.His196Gln
|
|
XM_006711270.1:c.735C>A
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XP_006711333.1:p.His245Gln
|
|
XM_011509407.1:c.735C>A
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XP_011507709.1:p.His245Gln
|
|
NM_000157.4:c.735C>A
MANE Select
|
NP_000148.2:p.His245Gln
|
|
NM_001005741.3:c.735C>A
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NP_001005741.1:p.His245Gln
|
|
NM_001005742.3:c.735C>A
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NP_001005742.1:p.His245Gln
|
|
NM_001171811.2:c.474C>A
|
NP_001165282.1:p.His158Gln
|
|
NM_001171812.2:c.588C>A
|
NP_001165283.1:p.His196Gln
|
|