ENST00000269187.10:c.1467A>T
MANE Select
|
ENSP00000269187.4:p.Arg489=
|
|
ENST00000269187.9:c.1467A>T
|
ENSP00000269187.4:p.Arg489=
|
|
ENST00000440549.6:c.642A>T
|
ENSP00000401139.1:p.Arg214=
|
|
ENST00000586829.1:c.168A>T
|
ENSP00000467724.1:p.Arg56=
|
|
ENST00000590986.5:c.1467A>T
|
ENSP00000465915.1:p.Arg489=
|
|
NM_001099406.1:c.642A>T
|
NP_001092876.1:p.Arg214=
|
|
NM_012319.3:c.1467A>T
|
NP_036451.3:p.Arg489=
|
|
XM_011525900.1:c.1467A>T
|
XP_011524202.1:p.Arg489=
|
|
XM_011525901.1:c.1467A>T
|
XP_011524203.1:p.Arg489=
|
|
XM_011525900.2:c.1467A>T
|
XP_011524202.1:p.Arg489=
|
|
XM_011525901.2:c.1467A>T
|
XP_011524203.1:p.Arg489=
|
|
NM_012319.4:c.1467A>T
MANE Select
|
NP_036451.4:p.Arg489=
|
|
NM_001099406.2:c.642A>T
|
NP_001092876.1:p.Arg214=
|
|