ENST00000281928.9:c.3316G>T
MANE Select
|
ENSP00000281928.3:p.Ala1106Ser
|
|
ENST00000549786.2:c.2744G>T
|
|
|
ENST00000648379.1:n.1684G>T
|
|
|
ENST00000648737.1:n.3080G>T
|
|
|
ENST00000648825.1:n.56G>T
|
|
|
ENST00000648916.1:n.1327G>T
|
|
|
ENST00000649607.1:c.1500G>T
|
|
|
ENST00000650226.1:c.3316G>T
|
ENSP00000496981.1:p.Ala1106Ser
|
|
ENST00000281928.7:c.3316G>T
|
ENSP00000281928.3:p.Ala1106Ser
|
|
NM_015335.4:c.3316G>T
|
NP_056150.1:p.Ala1106Ser
|
|
XM_011538080.1:c.3316G>T
|
XP_011536382.1:p.Ala1106Ser
|
|
XM_011538081.1:c.3313G>T
|
XP_011536383.1:p.Ala1105Ser
|
|
XM_011538082.1:c.3286G>T
|
XP_011536384.1:p.Ala1096Ser
|
|
XM_011538080.2:c.3316G>T
|
XP_011536382.1:p.Ala1106Ser
|
|
XM_011538081.2:c.3313G>T
|
XP_011536383.1:p.Ala1105Ser
|
|
XM_011538082.2:c.3286G>T
|
XP_011536384.1:p.Ala1096Ser
|
|
XM_017019090.1:c.3313G>T
|
XP_016874579.1:p.Ala1105Ser
|
|
NM_015335.5:c.3316G>T
MANE Select
|
NP_056150.1:p.Ala1106Ser
|
|