ENST00000318312.12:c.28G>C
MANE Select
|
ENSP00000317469.7:p.Asp10His
|
|
ENST00000318312.11:c.28G>C
|
ENSP00000317469.7:p.Asp10His
|
|
ENST00000393994.4:c.28G>C
|
ENSP00000377563.2:p.Asp10His
|
|
ENST00000419755.3:c.159-326G>C
|
ENSP00000398526.3:n.159-326G>C
|
|
ENST00000455748.6:c.28G>C
|
ENSP00000405764.2:p.Asp10His
|
|
ENST00000524907.5:n.18G>C
|
|
|
ENST00000525809.5:c.28G>C
|
ENSP00000431187.1:p.Asp10His
|
|
ENST00000526035.5:c.28G>C
|
ENSP00000434197.1:p.Asp10His
|
|
ENST00000526760.5:c.28G>C
|
ENSP00000432140.1:p.Asp10His
|
|
ENST00000526815.5:c.-369G>C
|
ENSP00000436860.1:n.-369G>C
|
|
ENST00000527251.5:c.-369G>C
|
ENSP00000434360.1:n.-369G>C
|
|
ENST00000529766.5:n.35G>C
|
|
|
ENST00000529955.5:n.46G>C
|
|
|
ENST00000532908.5:c.28G>C
|
ENSP00000431866.1:p.Asp10His
|
|
ENST00000533557.5:c.28G>C
|
ENSP00000434619.1:p.Asp10His
|
|
ENST00000533644.5:c.28G>C
|
ENSP00000436073.1:p.Asp10His
|
|
ENST00000534730.5:n.40G>C
|
|
|
ENST00000630659.2:c.28G>C
|
ENSP00000486455.1:p.Asp10His
|
|
NM_024649.4:c.28G>C
|
NP_078925.3:p.Asp10His
|
|
NM_024649.5:c.28G>C
MANE Select
|
NP_078925.3:p.Asp10His
|
|