ENST00000593677.2:c.1841T>C
|
|
|
ENST00000688602.1:c.3238T>C
|
|
|
ENST00000689936.1:c.3210T>C
|
|
|
ENST00000692547.1:n.298T>C
|
|
|
ENST00000359596.8:c.14905T>C
MANE Select
|
ENSP00000352608.2:p.Phe4969Leu
|
|
ENST00000355481.8:c.14890T>C
|
ENSP00000347667.3:p.Phe4964Leu
|
|
ENST00000359596.7:c.14905T>C
|
ENSP00000352608.2:p.Phe4969Leu
|
|
ENST00000360985.7:c.14887T>C
|
ENSP00000354254.4:p.Phe4963Leu
|
|
NM_000540.2:c.14905T>C , LRG_766t1:c.14905T>C
|
NP_000531.2:p.Phe4969Leu
|
|
NM_001042723.1:c.14890T>C
|
NP_001036188.1:p.Phe4964Leu
|
|
XM_006723317.1:c.14887T>C
|
XP_006723380.1:p.Phe4963Leu
|
|
XM_006723319.1:c.14872T>C
|
XP_006723382.1:p.Phe4958Leu
|
|
XM_011527204.1:c.14902T>C
|
XP_011525506.1:p.Phe4968Leu
|
|
XM_011527205.1:c.14818T>C
|
XP_011525507.1:p.Phe4940Leu
|
|
XM_006723317.2:c.14887T>C
|
XP_006723380.1:p.Phe4963Leu
|
|
XM_006723319.2:c.14872T>C
|
XP_006723382.1:p.Phe4958Leu
|
|
XM_011527205.2:c.14818T>C
|
XP_011525507.1:p.Phe4940Leu
|
|
NM_000540.3:c.14905T>C
MANE Select
|
NP_000531.2:p.Phe4969Leu
|
|
NM_001042723.2:c.14890T>C
|
NP_001036188.1:p.Phe4964Leu
|
|