ENST00000318312.12:c.212T>C
MANE Select
|
ENSP00000317469.7:p.Leu71Pro
|
|
ENST00000318312.11:c.212T>C
|
ENSP00000317469.7:p.Leu71Pro
|
|
ENST00000393994.4:c.212T>C
|
ENSP00000377563.2:p.Leu71Pro
|
|
ENST00000419755.3:c.323T>C
|
ENSP00000398526.3:p.Leu108Pro
|
|
ENST00000455748.6:c.212T>C
|
ENSP00000405764.2:p.Leu71Pro
|
|
ENST00000524458.5:c.87T>C
|
ENSP00000436195.1:p.Ala29=
|
|
ENST00000524705.2:c.-20-48T>C
|
ENSP00000436927.1:n.-20-48T>C
|
|
ENST00000524907.5:n.202T>C
|
|
|
ENST00000525809.5:c.160-1082T>C
|
ENSP00000431187.1:n.160-1082T>C
|
|
ENST00000526035.5:c.177T>C
|
ENSP00000434197.1:p.Ala59=
|
|
ENST00000526760.5:c.177T>C
|
ENSP00000432140.1:p.Ala59=
|
|
ENST00000526815.5:c.122T>C
|
ENSP00000436860.1:p.Leu41Pro
|
|
ENST00000527251.5:c.87T>C
|
ENSP00000434360.1:p.Ala29=
|
|
ENST00000529766.5:n.219T>C
|
|
|
ENST00000529955.5:n.230T>C
|
|
|
ENST00000532908.5:c.177T>C
|
ENSP00000431866.1:p.Ala59=
|
|
ENST00000533557.5:c.177T>C
|
ENSP00000434619.1:p.Ala59=
|
|
ENST00000533644.5:c.212T>C
|
ENSP00000436073.1:p.Leu71Pro
|
|
ENST00000534730.5:n.224T>C
|
|
|
ENST00000630659.2:c.177T>C
|
ENSP00000486455.1:p.Ala59=
|
|
NM_024649.4:c.212T>C
|
NP_078925.3:p.Leu71Pro
|
|
NM_024649.5:c.212T>C
MANE Select
|
NP_078925.3:p.Leu71Pro
|
|