ENST00000593677.2:c.900C>T
|
|
|
ENST00000688602.1:c.2297C>T
|
|
|
ENST00000689936.1:c.2269C>T
|
|
|
ENST00000359596.8:c.13964C>T
MANE Select
|
ENSP00000352608.2:p.Ala4655Val
|
|
ENST00000355481.8:c.13949C>T
|
ENSP00000347667.3:p.Ala4650Val
|
|
ENST00000359596.7:c.13964C>T
|
ENSP00000352608.2:p.Ala4655Val
|
|
ENST00000360985.7:c.13946C>T
|
ENSP00000354254.4:p.Ala4649Val
|
|
ENST00000593677.1:c.424C>T
|
|
|
NM_000540.2:c.13964C>T , LRG_766t1:c.13964C>T
|
NP_000531.2:p.Ala4655Val
|
|
NM_001042723.1:c.13949C>T
|
NP_001036188.1:p.Ala4650Val
|
|
XM_006723317.1:c.13946C>T
|
XP_006723380.1:p.Ala4649Val
|
|
XM_006723319.1:c.13931C>T
|
XP_006723382.1:p.Ala4644Val
|
|
XM_011527204.1:c.13961C>T
|
XP_011525506.1:p.Ala4654Val
|
|
XM_011527205.1:c.13877C>T
|
XP_011525507.1:p.Ala4626Val
|
|
XM_006723317.2:c.13946C>T
|
XP_006723380.1:p.Ala4649Val
|
|
XM_006723319.2:c.13931C>T
|
XP_006723382.1:p.Ala4644Val
|
|
XM_011527205.2:c.13877C>T
|
XP_011525507.1:p.Ala4626Val
|
|
NM_000540.3:c.13964C>T
MANE Select
|
NP_000531.2:p.Ala4655Val
|
|
NM_001042723.2:c.13949C>T
|
NP_001036188.1:p.Ala4650Val
|
|