ENST00000593677.2:c.1814T>G
|
|
|
ENST00000688602.1:c.3211T>G
|
|
|
ENST00000689936.1:c.3183T>G
|
|
|
ENST00000692547.1:n.271T>G
|
|
|
ENST00000359596.8:c.14878T>G
MANE Select
|
ENSP00000352608.2:p.Phe4960Val
|
|
ENST00000355481.8:c.14863T>G
|
ENSP00000347667.3:p.Phe4955Val
|
|
ENST00000359596.7:c.14878T>G
|
ENSP00000352608.2:p.Phe4960Val
|
|
ENST00000360985.7:c.14860T>G
|
ENSP00000354254.4:p.Phe4954Val
|
|
NM_000540.2:c.14878T>G , LRG_766t1:c.14878T>G
|
NP_000531.2:p.Phe4960Val
|
|
NM_001042723.1:c.14863T>G
|
NP_001036188.1:p.Phe4955Val
|
|
XM_006723317.1:c.14860T>G
|
XP_006723380.1:p.Phe4954Val
|
|
XM_006723319.1:c.14845T>G
|
XP_006723382.1:p.Phe4949Val
|
|
XM_011527204.1:c.14875T>G
|
XP_011525506.1:p.Phe4959Val
|
|
XM_011527205.1:c.14791T>G
|
XP_011525507.1:p.Phe4931Val
|
|
XM_006723317.2:c.14860T>G
|
XP_006723380.1:p.Phe4954Val
|
|
XM_006723319.2:c.14845T>G
|
XP_006723382.1:p.Phe4949Val
|
|
XM_011527205.2:c.14791T>G
|
XP_011525507.1:p.Phe4931Val
|
|
NM_000540.3:c.14878T>G
MANE Select
|
NP_000531.2:p.Phe4960Val
|
|
NM_001042723.2:c.14863T>G
|
NP_001036188.1:p.Phe4955Val
|
|