|
ENST00000277225.10:c.3787C>T
MANE Select
|
ENSP00000277225.5:p.Arg1263Ter
|
|
|
ENST00000277225.9:c.3787C>T
|
ENSP00000277225.5:p.Arg1263Ter
|
|
|
ENST00000374686.6:c.436C>T
|
ENSP00000363818.2:p.Arg146Ter
|
|
|
ENST00000441147.6:c.322C>T
|
ENSP00000397306.2:p.Arg108Ter
|
|
|
ENST00000472574.1:c.281-2826C>T
|
ENSP00000476222.1:n.281-2826C>T
|
|
|
ENST00000480607.5:n.240+535C>T
|
|
|
|
NM_021224.4:c.3787C>T
|
NP_067047.4:p.Arg1263Ter
|
|
|
XM_006717209.2:c.3787C>T
|
XP_006717272.1:p.Arg1263Ter
|
|
|
XM_006717210.2:c.3787C>T
|
XP_006717273.1:p.Arg1263Ter
|
|
|
XM_006717211.2:c.3787C>T
|
XP_006717274.1:p.Arg1263Ter
|
|
|
XM_006717212.2:c.3787C>T
|
XP_006717275.1:p.Arg1263Ter
|
|
|
XM_006717215.2:c.3787C>T
|
XP_006717278.1:p.Arg1263Ter
|
|
|
XM_006717216.2:c.3787C>T
|
XP_006717279.1:p.Arg1263Ter
|
|
|
XM_006717218.2:c.3252+535C>T
|
XP_006717281.1:n.3252+535C>T
|
|
|
XM_011518892.1:c.3787C>T
|
XP_011517194.1:p.Arg1263Ter
|
|
|
NM_001347997.1:c.3252+535C>T
|
NP_001334926.1:n.3252+535C>T
|
|
|
NM_021224.5:c.3787C>T
|
NP_067047.4:p.Arg1263Ter
|
|
|
XM_006717209.4:c.3787C>T
|
XP_006717272.1:p.Arg1263Ter
|
|
|
XM_006717211.4:c.3787C>T
|
XP_006717274.1:p.Arg1263Ter
|
|
|
XM_006717212.4:c.3787C>T
|
XP_006717275.1:p.Arg1263Ter
|
|
|
XM_006717215.4:c.3787C>T
|
XP_006717278.1:p.Arg1263Ter
|
|
|
XM_006717216.4:c.3787C>T
|
XP_006717279.1:p.Arg1263Ter
|
|
|
XM_006717218.4:c.3252+535C>T
|
XP_006717281.1:n.3252+535C>T
|
|
|
XM_017014996.2:c.3787C>T
|
XP_016870485.1:p.Arg1263Ter
|
|
|
XM_017014997.2:c.3787C>T
|
XP_016870486.1:p.Arg1263Ter
|
|
|
XM_017014998.2:c.3252+535C>T
|
XP_016870487.1:n.3252+535C>T
|
|
|
XM_024447629.1:c.3787C>T
|
XP_024303397.1:p.Arg1263Ter
|
|
|
NM_021224.6:c.3787C>T
MANE Select
|
NP_067047.4:p.Arg1263Ter
|
|
|
NM_001347997.2:c.3252+535C>T
|
NP_001334926.1:n.3252+535C>T
|
|
