ENST00000377833.10:c.10850T>C
MANE Select
|
ENSP00000367064.4:p.Phe3617Ser
|
|
ENST00000377833.8:c.10850T>C
|
ENSP00000367064.4:p.Phe3617Ser
|
|
NM_001081.3:c.10850T>C , LRG_540t1:c.10850T>C
|
NP_001072.2:p.Phe3617Ser
|
|
XM_011519709.1:c.6836T>C
|
XP_011518011.1:p.Phe2279Ser
|
|
XM_011519710.1:c.6812T>C
|
XP_011518012.1:p.Phe2271Ser
|
|
XM_011519711.1:c.6692T>C
|
XP_011518013.1:p.Phe2231Ser
|
|
XM_011519709.2:c.6836T>C
|
XP_011518011.1:p.Phe2279Ser
|
|
XM_011519710.2:c.6812T>C
|
XP_011518012.1:p.Phe2271Ser
|
|
XM_011519711.3:c.6692T>C
|
XP_011518013.1:p.Phe2231Ser
|
|
NM_001081.4:c.10850T>C
MANE Select
|
NP_001072.2:p.Phe3617Ser
|
|