ENST00000593677.2:c.1675C>G
|
|
|
ENST00000688602.1:c.3072C>G
|
|
|
ENST00000689936.1:c.3044C>G
|
|
|
ENST00000692547.1:n.132C>G
|
|
|
ENST00000359596.8:c.14739C>G
MANE Select
|
ENSP00000352608.2:p.Tyr4913Ter
|
|
ENST00000355481.8:c.14724C>G
|
ENSP00000347667.3:p.Tyr4908Ter
|
|
ENST00000359596.7:c.14739C>G
|
ENSP00000352608.2:p.Tyr4913Ter
|
|
ENST00000360985.7:c.14721C>G
|
ENSP00000354254.4:p.Tyr4907Ter
|
|
NM_000540.2:c.14739C>G , LRG_766t1:c.14739C>G
|
NP_000531.2:p.Tyr4913Ter
|
|
NM_001042723.1:c.14724C>G
|
NP_001036188.1:p.Tyr4908Ter
|
|
XM_006723317.1:c.14721C>G
|
XP_006723380.1:p.Tyr4907Ter
|
|
XM_006723319.1:c.14706C>G
|
XP_006723382.1:p.Tyr4902Ter
|
|
XM_011527204.1:c.14736C>G
|
XP_011525506.1:p.Tyr4912Ter
|
|
XM_011527205.1:c.14652C>G
|
XP_011525507.1:p.Tyr4884Ter
|
|
XM_006723317.2:c.14721C>G
|
XP_006723380.1:p.Tyr4907Ter
|
|
XM_006723319.2:c.14706C>G
|
XP_006723382.1:p.Tyr4902Ter
|
|
XM_011527205.2:c.14652C>G
|
XP_011525507.1:p.Tyr4884Ter
|
|
NM_000540.3:c.14739C>G
MANE Select
|
NP_000531.2:p.Tyr4913Ter
|
|
NM_001042723.2:c.14724C>G
|
NP_001036188.1:p.Tyr4908Ter
|
|