ENST00000302068.9:c.1072G>C
MANE Select
|
ENSP00000306099.4:p.Gly358Arg
|
|
ENST00000302068.8:c.1072G>C
|
ENSP00000306099.4:p.Gly358Arg
|
|
ENST00000502545.5:n.939+320G>C
|
|
|
ENST00000509493.1:c.415G>C
|
ENSP00000426757.1:p.Gly139Arg
|
|
NM_001184741.1:c.895G>C
|
NP_001171670.1:p.Gly299Arg
|
|
NM_005141.4:c.1072G>C , LRG_558t1:c.1072G>C
|
NP_005132.2:p.Gly358Arg
|
|
NM_001382759.1:c.940G>C
|
NP_001369688.1:p.Gly314Arg
|
|
NM_001382760.1:c.1072G>C
|
NP_001369689.1:p.Gly358Arg
|
|
NM_001382761.1:c.1072G>C
|
NP_001369690.1:p.Gly358Arg
|
|
NM_001382762.1:c.772G>C
|
NP_001369691.1:p.Gly258Arg
|
|
NM_001382763.1:c.1063G>C
|
NP_001369692.1:p.Gly355Arg
|
|
NM_001382764.1:c.1072G>C
|
NP_001369693.1:p.Gly358Arg
|
|
NM_001382765.1:c.1072G>C
|
NP_001369694.1:p.Gly358Arg
|
|
NM_005141.5:c.1072G>C
MANE Select
|
NP_005132.2:p.Gly358Arg
|
|