|
ENST00000362012.7:c.54G>T
MANE Select
|
ENSP00000354612.2:p.Pro18=
|
|
|
ENST00000426608.6:c.54G>T
|
ENSP00000411606.2:p.Pro18=
|
|
|
ENST00000540753.6:c.-244G>T
|
ENSP00000437709.1:n.-244G>T
|
|
|
ENST00000619306.5:c.54G>T
|
ENSP00000483540.2:p.Pro18=
|
|
|
ENST00000643576.1:n.148G>T
|
|
|
|
ENST00000643810.1:c.-274G>T
|
ENSP00000494717.1:n.-274G>T
|
|
|
ENST00000645132.1:n.221G>T
|
|
|
|
ENST00000647067.1:c.54G>T
|
ENSP00000495728.1:p.Pro18=
|
|
|
ENST00000223423.8:c.54G>T
|
ENSP00000223423.4:p.Pro18=
|
|
|
ENST00000362012.6:c.54G>T
|
ENSP00000354612.2:p.Pro18=
|
|
|
ENST00000426608.5:c.45G>T
|
ENSP00000411606.1:p.Pro15=
|
|
|
ENST00000540753.5:c.-244G>T
|
ENSP00000437709.1:n.-244G>T
|
|
|
ENST00000614910.4:c.54G>T
|
ENSP00000484800.1:p.Pro18=
|
|
|
ENST00000619306.4:c.147G>T
|
ENSP00000483540.1:p.Pro49=
|
|
|
NM_000962.3:c.54G>T
|
NP_000953.2:p.Pro18=
|
|
|
NM_001271164.1:c.54G>T
|
NP_001258093.1:p.Pro18=
|
|
|
NM_001271166.1:c.-274G>T
|
NP_001258095.1:n.-274G>T
|
|
|
NM_001271367.1:c.-245G>T
|
NP_001258296.1:n.-245G>T
|
|
|
NM_001271368.1:c.-244G>T
|
NP_001258297.1:n.-244G>T
|
|
|
NM_080591.2:c.54G>T
|
NP_542158.1:p.Pro18=
|
|
|
XM_005252105.2:c.-244G>T
|
XP_005252162.1:n.-244G>T
|
|
|
XM_011518875.1:c.-244G>T
|
XP_011517177.1:n.-244G>T
|
|
|
XM_011518876.1:c.-4106G>T
|
XP_011517178.1:n.-4106G>T
|
|
|
XM_005252105.3:c.-244G>T
|
XP_005252162.1:n.-244G>T
|
|
|
XM_011518875.2:c.-244G>T
|
XP_011517177.1:n.-244G>T
|
|
|
XM_011518876.2:c.-4106G>T
|
XP_011517178.1:n.-4106G>T
|
|
|
XM_024447614.1:c.-274G>T
|
XP_024303382.1:n.-274G>T
|
|
|
XM_024447615.1:c.-274G>T
|
XP_024303383.1:n.-274G>T
|
|
|
NM_000962.4:c.54G>T
MANE Select
|
NP_000953.2:p.Pro18=
|
|
|
NM_001271164.2:c.54G>T
|
NP_001258093.1:p.Pro18=
|
|
|
NM_001271166.2:c.-274G>T
|
NP_001258095.1:n.-274G>T
|
|
|
NM_001271367.2:c.-245G>T
|
NP_001258296.1:n.-245G>T
|
|
|
NM_001271368.2:c.-244G>T
|
NP_001258297.1:n.-244G>T
|
|
|
NM_080591.3:c.54G>T
|
NP_542158.1:p.Pro18=
|
|
