ENST00000411466.7:c.7342G>T
|
ENSP00000405186.3:p.Ala2448Ser
|
|
ENST00000704023.1:c.1593+29G>T
|
|
|
ENST00000706321.1:c.7342G>T
|
ENSP00000516346.1:p.Ala2448Ser
|
|
ENST00000262518.9:c.7342G>T
MANE Select
|
ENSP00000262518.4:p.Ala2448Ser
|
|
ENST00000262518.8:c.7342G>T
|
ENSP00000262518.4:p.Ala2448Ser
|
|
ENST00000380361.7:c.6811G>T
|
ENSP00000369719.3:p.Ala2271Ser
|
|
ENST00000395059.6:c.6565G>T
|
ENSP00000378499.3:p.Ala2189Ser
|
|
NM_006662.2:c.7342G>T
|
NP_006653.2:p.Ala2448Ser
|
|
NM_006662.3:c.7342G>T
MANE Select
|
NP_006653.2:p.Ala2448Ser
|
|