ENST00000219478.11:c.652G>T
MANE Select
|
ENSP00000219478.5:p.Ala218Ser
|
|
ENST00000219478.10:c.652G>T
|
ENSP00000219478.5:p.Ala218Ser
|
|
ENST00000545009.1:c.652G>T
|
ENSP00000445714.1:p.Ala218Ser
|
|
ENST00000589422.1:c.*180G>T
|
ENSP00000466375.1:n.*180G>T
|
|
NM_001303450.1:c.652G>T
|
NP_001290379.1:p.Ala218Ser
|
|
NM_021646.2:c.652G>T
|
NP_067678.1:p.Ala218Ser
|
|
XM_005255243.2:c.301G>T
|
XP_005255300.1:p.Ala101Ser
|
|
XM_011522453.1:c.652G>T
|
XP_011520755.1:p.Ala218Ser
|
|
XM_011522454.1:c.28G>T
|
XP_011520756.1:p.Ala10Ser
|
|
NM_021646.3:c.652G>T
|
NP_067678.1:p.Ala218Ser
|
|
XM_005255243.4:c.301G>T
|
XP_005255300.1:p.Ala101Ser
|
|
XM_011522453.2:c.652G>T
|
XP_011520755.1:p.Ala218Ser
|
|
XM_011522454.3:c.28G>T
|
XP_011520756.1:p.Ala10Ser
|
|
XM_017023121.2:c.28G>T
|
XP_016878610.1:p.Ala10Ser
|
|
NM_001303450.2:c.652G>T
|
NP_001290379.1:p.Ala218Ser
|
|
NM_021646.4:c.652G>T
MANE Select
|
NP_067678.1:p.Ala218Ser
|
|