ENST00000272895.12:c.1493T>C
MANE Select
|
ENSP00000272895.7:p.Val498Ala
|
|
ENST00000272895.11:c.1493T>C
|
ENSP00000272895.7:p.Val498Ala
|
|
ENST00000389661.4:c.539T>C
|
ENSP00000374312.4:p.Val180Ala
|
|
NM_015657.3:c.539T>C
|
NP_056472.2:p.Val180Ala
|
|
NM_173076.2:c.1493T>C
|
NP_775099.2:p.Val498Ala
|
|
NR_103740.1:n.1737T>C
|
|
|
XM_011510951.1:c.1493T>C
|
XP_011509253.1:p.Val498Ala
|
|
XM_011510952.1:c.1493T>C
|
XP_011509254.1:p.Val498Ala
|
|
XM_011510951.2:c.1493T>C
|
XP_011509253.1:p.Val498Ala
|
|
NM_173076.3:c.1493T>C
MANE Select
|
NP_775099.2:p.Val498Ala
|
|
NR_103740.2:n.1935T>C
|
|
|
NM_015657.4:c.539T>C
|
NP_056472.2:p.Val180Ala
|
|