ENST00000269187.10:c.1480T>C
MANE Select
|
ENSP00000269187.4:p.Leu494=
|
|
ENST00000269187.9:c.1480T>C
|
ENSP00000269187.4:p.Leu494=
|
|
ENST00000440549.6:c.655T>C
|
ENSP00000401139.1:p.Leu219=
|
|
ENST00000586829.1:c.181T>C
|
ENSP00000467724.1:p.Leu61=
|
|
ENST00000590986.5:c.1480T>C
|
ENSP00000465915.1:p.Leu494=
|
|
NM_001099406.1:c.655T>C
|
NP_001092876.1:p.Leu219=
|
|
NM_012319.3:c.1480T>C
|
NP_036451.3:p.Leu494=
|
|
XM_011525900.1:c.1480T>C
|
XP_011524202.1:p.Leu494=
|
|
XM_011525901.1:c.1480T>C
|
XP_011524203.1:p.Leu494=
|
|
XM_011525900.2:c.1480T>C
|
XP_011524202.1:p.Leu494=
|
|
XM_011525901.2:c.1480T>C
|
XP_011524203.1:p.Leu494=
|
|
NM_012319.4:c.1480T>C
MANE Select
|
NP_036451.4:p.Leu494=
|
|
NM_001099406.2:c.655T>C
|
NP_001092876.1:p.Leu219=
|
|