ENST00000367990.7:c.192C>G
MANE Select
|
ENSP00000356969.3:p.Tyr64Ter
|
|
ENST00000463273.5:c.192C>G
|
ENSP00000476740.1:p.Tyr64Ter
|
|
ENST00000463812.1:c.48C>G
|
ENSP00000476890.1:p.Tyr16Ter
|
|
ENST00000464492.5:c.291C>G
|
ENSP00000476911.1:p.Tyr97Ter
|
|
ENST00000468465.5:c.48C>G
|
ENSP00000476662.1:p.Tyr16Ter
|
|
ENST00000469730.2:c.192C>G
|
ENSP00000476605.1:p.Tyr64Ter
|
|
ENST00000470459.6:c.192C>G
|
ENSP00000477031.1:p.Tyr64Ter
|
|
ENST00000481413.1:n.703C>G
|
|
|
ENST00000481511.5:c.*189C>G
|
ENSP00000477054.1:n.*189C>G
|
|
ENST00000491350.1:c.59C>G
|
ENSP00000477353.1:p.Thr20Ser
|
|
NM_001643.1:c.192C>G
|
NP_001634.1:p.Tyr64Ter
|
|
NM_001643.2:c.192C>G
MANE Select
|
NP_001634.1:p.Tyr64Ter
|
|