ENST00000361915.8:c.2091C>G
MANE Select
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ENSP00000355106.3:p.Gly697=
|
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ENST00000637337.1:n.2302C>G
|
|
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ENST00000294724.8:c.2091C>G
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ENSP00000294724.4:p.Gly697=
|
|
ENST00000361302.7:c.2043C>G
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ENSP00000354971.3:p.Gly681=
|
|
ENST00000361522.4:c.2040C>G
|
ENSP00000354635.4:p.Gly680=
|
|
ENST00000361915.7:c.2091C>G
|
ENSP00000355106.3:p.Gly697=
|
|
ENST00000370161.6:c.2043C>G
|
ENSP00000359180.2:p.Gly681=
|
|
ENST00000370163.7:c.2091C>G
|
ENSP00000359182.3:p.Gly697=
|
|
ENST00000370165.7:c.2091C>G
|
ENSP00000359184.3:p.Gly697=
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|
NM_000028.2:c.2091C>G
|
NP_000019.2:p.Gly697=
|
|
NM_000642.2:c.2091C>G
|
NP_000633.2:p.Gly697=
|
|
NM_000643.2:c.2091C>G
|
NP_000634.2:p.Gly697=
|
|
NM_000644.2:c.2091C>G
|
NP_000635.2:p.Gly697=
|
|
NM_000645.2:c.2040C>G
|
NP_000636.2:p.Gly680=
|
|
NM_000646.2:c.2043C>G
|
NP_000637.2:p.Gly681=
|
|
XM_005270557.1:c.2091C>G
|
XP_005270614.1:p.Gly697=
|
|
XM_005270557.2:c.2091C>G
|
XP_005270614.1:p.Gly697=
|
|
XM_017000501.2:c.351C>G
|
XP_016855990.1:p.Gly117=
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|
NM_000642.3:c.2091C>G
MANE Select
|
NP_000633.2:p.Gly697=
|
|