ENST00000593677.2:c.1466C>G
|
|
|
ENST00000688602.1:c.2863C>G
|
|
|
ENST00000689936.1:c.2835C>G
|
|
|
ENST00000359596.8:c.14530C>G
MANE Select
|
ENSP00000352608.2:p.Leu4844Val
|
|
ENST00000355481.8:c.14515C>G
|
ENSP00000347667.3:p.Leu4839Val
|
|
ENST00000359596.7:c.14530C>G
|
ENSP00000352608.2:p.Leu4844Val
|
|
ENST00000360985.7:c.14512C>G
|
ENSP00000354254.4:p.Leu4838Val
|
|
NM_000540.2:c.14530C>G , LRG_766t1:c.14530C>G
|
NP_000531.2:p.Leu4844Val
|
|
NM_001042723.1:c.14515C>G
|
NP_001036188.1:p.Leu4839Val
|
|
XM_006723317.1:c.14512C>G
|
XP_006723380.1:p.Leu4838Val
|
|
XM_006723319.1:c.14497C>G
|
XP_006723382.1:p.Leu4833Val
|
|
XM_011527204.1:c.14527C>G
|
XP_011525506.1:p.Leu4843Val
|
|
XM_011527205.1:c.14443C>G
|
XP_011525507.1:p.Leu4815Val
|
|
XM_006723317.2:c.14512C>G
|
XP_006723380.1:p.Leu4838Val
|
|
XM_006723319.2:c.14497C>G
|
XP_006723382.1:p.Leu4833Val
|
|
XM_011527205.2:c.14443C>G
|
XP_011525507.1:p.Leu4815Val
|
|
NM_000540.3:c.14530C>G
MANE Select
|
NP_000531.2:p.Leu4844Val
|
|
NM_001042723.2:c.14515C>G
|
NP_001036188.1:p.Leu4839Val
|
|