|
ENST00000356082.9:c.505C>T
MANE Select
|
ENSP00000348384.3:p.Gln169Ter
|
|
|
ENST00000356082.8:c.505C>T
|
ENSP00000348384.3:p.Gln169Ter
|
|
|
ENST00000367030.7:c.505C>T
|
ENSP00000355997.3:p.Gln169Ter
|
|
|
ENST00000391911.5:c.505C>T
|
ENSP00000375778.1:p.Gln169Ter
|
|
|
ENST00000415782.1:c.505C>T
|
ENSP00000388960.1:p.Gln169Ter
|
|
|
NM_000228.2:c.505C>T
|
NP_000219.2:p.Gln169Ter
|
|
|
NM_001017402.1:c.505C>T
|
NP_001017402.1:p.Gln169Ter
|
|
|
NM_001127641.1:c.505C>T
|
NP_001121113.1:p.Gln169Ter
|
|
|
XM_005273124.3:c.505C>T
|
XP_005273181.1:p.Gln169Ter
|
|
|
XM_005273124.4:c.505C>T
|
XP_005273181.1:p.Gln169Ter
|
|
|
XM_017001272.2:c.373-1373C>T
|
XP_016856761.1:n.373-1373C>T
|
|
|
NM_000228.3:c.505C>T
MANE Select
|
NP_000219.2:p.Gln169Ter
|
|
|
NM_001017402.2:c.505C>T
|
NP_001017402.1:p.Gln169Ter
|
|
