ENST00000682888.1:c.97C>T
|
ENSP00000508003.1:p.Gln33Ter
|
|
ENST00000683162.1:c.97C>T
|
ENSP00000508059.1:p.Gln33Ter
|
|
ENST00000683289.1:c.97C>T
|
ENSP00000508195.1:p.Gln33Ter
|
|
ENST00000683917.1:n.327C>T
|
|
|
ENST00000684356.1:c.97C>T
|
ENSP00000507619.1:p.Gln33Ter
|
|
ENST00000684745.1:n.1217C>T
|
|
|
ENST00000379374.5:c.1543C>T
MANE Select
|
ENSP00000368682.4:p.Gln515Ter
|
|
ENST00000379374.4:c.1543C>T
|
ENSP00000368682.4:p.Gln515Ter
|
|
NM_000444.5:c.1543C>T
|
NP_000435.3:p.Gln515Ter
|
|
NM_001282754.1:c.1543C>T
|
NP_001269683.1:p.Gln515Ter
|
|
XM_011545533.1:c.787C>T
|
XP_011543835.1:p.Gln263Ter
|
|
XM_011545534.1:c.787C>T
|
XP_011543836.1:p.Gln263Ter
|
|
XM_011545536.1:c.436C>T
|
XP_011543838.1:p.Gln146Ter
|
|
XM_011545536.2:c.436C>T
|
XP_011543838.1:p.Gln146Ter
|
|
XM_017029579.1:c.787C>T
|
XP_016885068.1:p.Gln263Ter
|
|
XM_024452390.1:c.1252C>T
|
XP_024308158.1:p.Gln418Ter
|
|
XR_001755695.1:n.2383C>T
|
|
|
NM_000444.6:c.1543C>T
MANE Select
|
NP_000435.3:p.Gln515Ter
|
|
NM_001282754.2:c.1543C>T
|
NP_001269683.1:p.Gln515Ter
|
|