ENST00000380776.5:n.184C>T
|
|
|
ENST00000496887.7:c.126C>T
|
ENSP00000434560.2:p.Val42=
|
|
ENST00000646564.2:c.387C>T
|
ENSP00000495806.2:p.Val129=
|
|
ENST00000155840.12:c.387C>T
MANE Select
|
ENSP00000155840.2:p.Val129=
|
|
ENST00000335475.6:c.6C>T
|
ENSP00000334497.5:p.Asp2=
|
|
ENST00000646564.1:c.33C>T
|
ENSP00000495806.1:p.Val11=
|
|
ENST00000155840.9:c.387C>T
|
ENSP00000155840.2:p.Val129=
|
|
ENST00000335475.5:c.6C>T
|
ENSP00000334497.5:p.Asp2=
|
|
ENST00000345015.4:n.256C>T
|
|
|
ENST00000380776.4:c.177C>T
|
ENSP00000370153.4:p.Gly59=
|
|
ENST00000496887.6:c.126C>T
|
ENSP00000434560.1:p.Val42=
|
|
NM_000218.2:c.387C>T , LRG_287t1:c.387C>T
|
NP_000209.2:p.Val129=
|
|
NM_181798.1:c.6C>T , LRG_287t2:c.6C>T
|
NP_861463.1:p.Asp2=
|
|
NM_000218.3:c.387C>T
MANE Select
|
NP_000209.2:p.Val129=
|
|