ENST00000376259.7:c.634G>C
MANE Select
|
ENSP00000365435.3:p.Gly212Arg
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|
ENST00000376259.6:c.634G>C
|
ENSP00000365435.3:p.Gly212Arg
|
|
ENST00000489921.1:n.346G>C
|
|
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ENST00000492361.1:n.623G>C
|
|
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NM_001066.2:c.634G>C
|
NP_001057.1:p.Gly212Arg
|
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XM_011542060.1:c.634G>C
|
XP_011540362.1:p.Gly212Arg
|
|
XM_011542061.1:c.634G>C
|
XP_011540363.1:p.Gly212Arg
|
|
XM_011542062.1:c.613G>C
|
XP_011540364.1:p.Gly205Arg
|
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XM_011542063.1:c.634G>C
|
XP_011540365.1:p.Gly212Arg
|
|
XM_011542060.2:c.634G>C
|
XP_011540362.1:p.Gly212Arg
|
|
XM_011542063.2:c.634G>C
|
XP_011540365.1:p.Gly212Arg
|
|
XM_017002211.1:c.634G>C
|
XP_016857700.1:p.Gly212Arg
|
|
XM_017002214.1:c.49G>C
|
XP_016857703.1:p.Gly17Arg
|
|
XM_017002215.1:c.49G>C
|
XP_016857704.1:p.Gly17Arg
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|
NM_001066.3:c.634G>C
MANE Select
|
NP_001057.1:p.Gly212Arg
|
|