NM_001330.5:c.319C>A
MANE Select
|
NP_001321.1:p.Arg107Ser
|
ENST00000279804.3:c.319C>A
MANE Select
|
ENSP00000279804.2:p.Arg107Ser
|
NM_001142544.1:c.316C>A
|
NP_001136016.1:p.Arg106Ser
|
NM_001142544.2:c.316C>A
|
NP_001136016.1:p.Arg106Ser
|
NM_001142544.3:c.316C>A
|
NP_001136016.1:p.Arg106Ser
|
NM_001330.3:c.319C>A , LRG_408t1:c.319C>A
|
NP_001321.1:p.Arg107Ser
|
NR_165660.1:n.457C>A
|
|
ENST00000279804.2:c.319C>A
|
ENSP00000279804.2:p.Arg107Ser
|
ENST00000395019.3:c.316C>A
|
ENSP00000378465.3:p.Arg106Ser
|
XM_011545759.1:c.385C>A
|
XP_011544061.1:p.Arg129Ser
|
XM_011545759.2:c.385C>A
|
XP_011544061.1:p.Arg129Ser
|
XM_011545760.1:c.343C>A
|
XP_011544062.1:p.Arg115Ser
|
XM_011545760.2:c.343C>A
|
XP_011544062.1:p.Arg115Ser
|