ENST00000513939.6:c.1083G=
|
ENSP00000424211.2:p.Glu361=
|
|
ENST00000616923.5:c.1038G=
|
ENSP00000482756.2:p.Glu346=
|
|
ENST00000643939.1:c.1203G=
|
ENSP00000495686.1:p.Glu401=
|
|
ENST00000650454.1:c.1197G=
MANE Select
|
ENSP00000497574.1:p.Glu399=
|
|
ENST00000229416.10:c.1197G=
|
ENSP00000229416.6:p.Glu399=
|
|
ENST00000504353.1:n.166G=
|
|
|
ENST00000509541.5:n.1642G=
|
|
|
ENST00000616923.4:c.1083G=
|
ENSP00000482756.1:p.Glu361=
|
|
NM_001197115.1:c.1083G=
|
NP_001184044.1:p.Glu361=
|
|
NM_001498.3:c.1197G=
|
NP_001489.1:p.Glu399=
|
|
NM_001498.4:c.1197G=
MANE Select
|
NP_001489.1:p.Glu399=
|
|
XM_017010749.1:c.486G=
|
XP_016866238.1:p.Glu162=
|
|
NM_001197115.2:c.1083G=
|
NP_001184044.1:p.Glu361=
|
|