ENST00000302068.9:c.1185G>T
MANE Select
|
ENSP00000306099.4:p.Arg395Ser
|
|
ENST00000302068.8:c.1185G>T
|
ENSP00000306099.4:p.Arg395Ser
|
|
ENST00000502545.5:n.939+433G>T
|
|
|
ENST00000509493.1:c.528G>T
|
ENSP00000426757.1:p.Arg176Ser
|
|
NM_001184741.1:c.1008G>T
|
NP_001171670.1:p.Arg336Ser
|
|
NM_005141.4:c.1185G>T , LRG_558t1:c.1185G>T
|
NP_005132.2:p.Arg395Ser
|
|
NM_001382759.1:c.1053G>T
|
NP_001369688.1:p.Arg351Ser
|
|
NM_001382760.1:c.1185G>T
|
NP_001369689.1:p.Arg395Ser
|
|
NM_001382761.1:c.1185G>T
|
NP_001369690.1:p.Arg395Ser
|
|
NM_001382762.1:c.885G>T
|
NP_001369691.1:p.Arg295Ser
|
|
NM_001382763.1:c.1176G>T
|
NP_001369692.1:p.Arg392Ser
|
|
NM_001382764.1:c.1081-33G>T
|
NP_001369693.1:n.1081-33G>T
|
|
NM_001382765.1:c.1185G>T
|
NP_001369694.1:p.Arg395Ser
|
|
NM_005141.5:c.1185G>T
MANE Select
|
NP_005132.2:p.Arg395Ser
|
|