ENST00000392492.8:c.335A>G
MANE Select
|
ENSP00000376282.2:p.His112Arg
|
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ENST00000250615.7:c.470A>G
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ENSP00000250615.2:p.His157Arg
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|
ENST00000392492.7:c.335A>G
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ENSP00000376282.2:p.His112Arg
|
|
ENST00000585649.1:c.449A>G
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ENSP00000468717.1:p.His150Arg
|
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ENST00000587798.1:c.*112A>G
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ENSP00000468239.1:n.*112A>G
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NM_001088.2:c.335A>G
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NP_001079.1:p.His112Arg
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|
NM_001166579.1:c.470A>G
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NP_001160051.1:p.His157Arg
|
|
NR_110548.1:n.646A>G
|
|
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XM_011524415.1:c.335A>G
|
XP_011522717.1:p.His112Arg
|
|
XM_011524416.1:c.542A>G
|
XP_011522718.1:p.His181Arg
|
|
XM_011524417.1:c.542A>G
|
XP_011522719.1:p.His181Arg
|
|
XM_011524418.1:c.542A>G
|
XP_011522720.1:p.His181Arg
|
|
XM_011524419.1:c.542A>G
|
XP_011522721.1:p.His181Arg
|
|
XM_011524420.1:c.542A>G
|
XP_011522722.1:p.His181Arg
|
|
XM_011524421.1:c.542A>G
|
XP_011522723.1:p.His181Arg
|
|
XM_011524422.1:c.425A>G
|
XP_011522724.1:p.His142Arg
|
|
XM_011524423.1:c.335A>G
|
XP_011522725.1:p.His112Arg
|
|
XM_017024259.1:c.449A>G
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XP_016879748.1:p.His150Arg
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NM_001088.3:c.335A>G
MANE Select
|
NP_001079.1:p.His112Arg
|
|
NR_110548.2:n.591A>G
|
|
|
NM_001166579.2:c.470A>G
|
NP_001160051.1:p.His157Arg
|
|