|
NM_000073.3:c.271C>T
MANE Select
|
NP_000064.1:p.Gln91Ter
|
|
ENST00000532917.3:c.271C>T
MANE Select
|
ENSP00000431445.2:p.Gln91Ter
|
|
NM_000073.2:c.271C>T , LRG_39t1:c.271C>T
|
NP_000064.1:p.Gln91Ter
|
|
ENST00000292144.8:c.*328C>T
|
ENSP00000292144.4:n.*328C>T
|
|
ENST00000392883.6:c.91C>T
|
ENSP00000376621.2:p.Gln31Ter
|
|
ENST00000527777.5:n.351C>T
|
|
|
ENST00000532903.1:n.347C>T
|
|
|
ENST00000532917.1:c.271C>T
|
ENSP00000431445.1:p.Gln91Ter
|
|
ENST00000533462.5:n.1043C>T
|
|
|
XM_005271724.2:c.271C>T
|
XP_005271781.1:p.Gln91Ter
|
|
XM_005271724.4:c.271C>T
|
XP_005271781.1:p.Gln91Ter
|
|
XM_006718941.2:c.271C>T
|
XP_006719004.1:p.Gln91Ter
|
|
XM_006718941.3:c.271C>T
|
XP_006719004.1:p.Gln91Ter
|