ENST00000223051.8:c.593T>G
MANE Select
|
ENSP00000223051.3:p.Val198Gly
|
|
ENST00000223051.7:c.593T>G
|
ENSP00000223051.3:p.Val198Gly
|
|
ENST00000431692.5:c.593T>G
|
ENSP00000413905.1:p.Val198Gly
|
|
ENST00000462107.1:c.593T>G
|
ENSP00000420525.1:p.Val198Gly
|
|
ENST00000465294.5:n.598T>G
|
|
|
ENST00000475011.1:n.122T>G
|
|
|
ENST00000476304.5:n.214T>G
|
|
|
NM_001206855.1:c.80T>G
|
NP_001193784.1:p.Val27Gly
|
|
NM_003227.3:c.593T>G
|
NP_003218.2:p.Val198Gly
|
|
XM_005250553.3:c.593T>G
|
XP_005250610.1:p.Val198Gly
|
|
XM_005250554.3:c.593T>G
|
XP_005250611.1:p.Val198Gly
|
|
NM_001206855.2:c.80T>G
|
NP_001193784.1:p.Val27Gly
|
|
XM_005250553.4:c.593T>G
|
XP_005250610.1:p.Val198Gly
|
|
XM_017012573.1:c.593T>G
|
XP_016868062.1:p.Val198Gly
|
|
NM_003227.4:c.593T>G
MANE Select
|
NP_003218.2:p.Val198Gly
|
|
NM_001206855.3:c.80T>G
|
NP_001193784.1:p.Val27Gly
|
|