ENST00000379958.3:c.2111_2112delinsCT
MANE Select
|
ENSP00000369292.2:p.Pro704=
|
|
ENST00000379958.2:c.2111_2112delinsCT
|
ENSP00000369292.2:p.Pro704=
|
|
ENST00000446617.1:c.2111_2112delinsCT
|
ENSP00000414529.1:p.Pro704=
|
|
ENST00000620985.4:c.2111_2112delinsCT
|
ENSP00000484636.1:p.Pro704=
|
|
NM_001193307.1:c.2111_2112delinsCT
|
NP_001180236.1:p.Pro704=
|
|
NM_017654.3:c.2111_2112delinsCT
|
NP_060124.2:p.Pro704=
|
|
NM_017654.4:c.2111_2112delinsCT
MANE Select
|
NP_060124.2:p.Pro704=
|
|
NM_001193307.2:c.2111_2112delinsCT
|
NP_001180236.1:p.Pro704=
|
|