ENST00000229771.11:c.1329T>C
MANE Select
|
ENSP00000229771.6:p.Ser443=
|
|
ENST00000229771.10:c.1329T>C
|
ENSP00000229771.6:p.Ser443=
|
|
ENST00000322263.8:c.1170T>C
|
ENSP00000319414.4:p.Ser390=
|
|
ENST00000495781.1:n.505T>C
|
|
|
ENST00000614066.4:c.1323T>C
|
ENSP00000477534.1:p.Ser441=
|
|
NM_001289395.1:c.1170T>C
|
NP_001276324.1:p.Ser390=
|
|
NM_003322.4:c.1329T>C
|
NP_003313.3:p.Ser443=
|
|
NM_003322.5:c.1329T>C
|
NP_003313.3:p.Ser443=
|
|
NM_003322.6:c.1329T>C
MANE Select
|
NP_003313.3:p.Ser443=
|
|
NM_001289395.2:c.1170T>C
|
NP_001276324.1:p.Ser390=
|
|