ENST00000262367.10:c.2059G>T
MANE Select
|
ENSP00000262367.5:p.Ala687Ser
|
|
ENST00000262367.9:c.2059G>T
|
ENSP00000262367.5:p.Ala687Ser
|
|
ENST00000382070.7:c.1945G>T
|
ENSP00000371502.3:p.Ala649Ser
|
|
ENST00000570939.2:c.664G>T
|
ENSP00000461002.2:p.Ala222Ser
|
|
ENST00000571826.5:c.108G>T
|
|
|
ENST00000572134.1:c.372G>T
|
|
|
ENST00000634839.1:n.221G>T
|
|
|
NM_001079846.1:c.1945G>T
|
NP_001073315.1:p.Ala649Ser
|
|
NM_004380.2:c.2059G>T
|
NP_004371.2:p.Ala687Ser
|
|
XM_005255124.3:c.2059G>T
|
XP_005255181.1:p.Ala687Ser
|
|
XM_005255125.3:c.2059G>T
|
XP_005255182.1:p.Ala687Ser
|
|
XM_006720848.2:c.2059G>T
|
XP_006720911.1:p.Ala687Ser
|
|
XM_011522380.1:c.2005G>T
|
XP_011520682.1:p.Ala669Ser
|
|
XM_011522381.1:c.1306G>T
|
XP_011520683.1:p.Ala436Ser
|
|
XM_011522382.1:c.2059G>T
|
XP_011520684.1:p.Ala687Ser
|
|
XM_005255124.4:c.2059G>T
|
XP_005255181.1:p.Ala687Ser
|
|
XM_005255125.4:c.2059G>T
|
XP_005255182.1:p.Ala687Ser
|
|
XM_006720848.3:c.2059G>T
|
XP_006720911.1:p.Ala687Ser
|
|
XM_011522381.2:c.1306G>T
|
XP_011520683.1:p.Ala436Ser
|
|
XM_011522382.3:c.2059G>T
|
XP_011520684.1:p.Ala687Ser
|
|
XM_017022944.1:c.2059G>T
|
XP_016878433.1:p.Ala687Ser
|
|
NM_004380.3:c.2059G>T
MANE Select
|
NP_004371.2:p.Ala687Ser
|
|