ENST00000334785.12:c.*80A>C
MANE Select
|
ENSP00000333938.7:n.*80A>C
|
|
ENST00000330010.12:c.*80A>C
|
ENSP00000327363.8:n.*80A>C
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|
ENST00000334785.11:c.*80A>C
|
ENSP00000333938.7:n.*80A>C
|
|
ENST00000342754.5:c.1726A>C
|
|
|
ENST00000480732.2:n.1682A>C
|
|
|
NM_001172309.1:c.*80A>C
|
NP_001165780.1:n.*80A>C
|
|
NM_144573.3:c.*80A>C , LRG_442t1:c.*80A>C
|
NP_653174.3:n.*80A>C
|
|
XM_005271322.2:c.2027A>C
|
XP_005271379.1:p.Tyr676Ser
|
|
XM_005271323.2:c.1985A>C
|
XP_005271380.1:p.Tyr662Ser
|
|
XM_005271324.3:c.1835A>C
|
XP_005271381.1:p.Tyr612Ser
|
|
XM_005271325.2:c.1805A>C
|
XP_005271382.1:p.Tyr602Ser
|
|
XM_005271326.2:c.1793A>C
|
XP_005271383.1:p.Tyr598Ser
|
|
XM_005271327.2:c.1610A>C
|
XP_005271384.1:p.Tyr537Ser
|
|
XM_005271322.4:c.2027A>C
|
XP_005271379.1:p.Tyr676Ser
|
|
XM_005271323.4:c.1985A>C
|
XP_005271380.1:p.Tyr662Ser
|
|
XM_005271324.5:c.1835A>C
|
XP_005271381.1:p.Tyr612Ser
|
|
XM_005271325.4:c.1805A>C
|
XP_005271382.1:p.Tyr602Ser
|
|
XM_005271326.4:c.1793A>C
|
XP_005271383.1:p.Tyr598Ser
|
|
XM_005271327.4:c.1610A>C
|
XP_005271384.1:p.Tyr537Ser
|
|
NM_001172309.2:c.*80A>C
|
NP_001165780.1:n.*80A>C
|
|
NM_144573.4:c.*80A>C
MANE Select
|
NP_653174.3:n.*80A>C
|
|