ENST00000692585.1:c.1095G>C
|
ENSP00000509200.1:p.Pro365=
|
|
ENST00000294309.8:c.2238G>C
MANE Select
|
ENSP00000294309.3:p.Pro746=
|
|
ENST00000635811.1:c.*433G>C
|
ENSP00000490341.1:n.*433G>C
|
|
ENST00000637084.1:c.1095G>C
|
ENSP00000490615.1:p.Pro365=
|
|
ENST00000637342.1:c.2003+2002G>C
|
ENSP00000490171.1:n.2003+2002G>C
|
|
ENST00000637504.1:c.*33+2646G>C
|
ENSP00000489759.1:n.*33+2646G>C
|
|
ENST00000294309.7:c.2238G>C
|
ENSP00000294309.3:p.Pro746=
|
|
ENST00000442692.2:n.1704G>C
|
|
|
ENST00000542467.1:c.1692G>C
|
ENSP00000445551.1:p.Pro564=
|
|
NM_139075.3:c.2238G>C
|
NP_620714.2:p.Pro746=
|
|
XM_005273824.2:c.2235G>C
|
XP_005273881.1:p.Pro745=
|
|
XM_005273826.2:c.1983G>C
|
XP_005273883.1:p.Pro661=
|
|
XM_005273830.2:c.1545G>C
|
XP_005273887.1:p.Pro515=
|
|
XM_005273831.2:c.1545G>C
|
XP_005273888.1:p.Pro515=
|
|
XM_005273832.2:c.1515G>C
|
XP_005273889.1:p.Pro505=
|
|
XM_006718453.2:c.1639+6433G>C
|
XP_006718516.1:n.1639+6433G>C
|
|
XM_006718454.2:c.1689+6433G>C
|
XP_006718517.1:n.1689+6433G>C
|
|
XM_011544802.1:c.1998G>C
|
XP_011543104.1:p.Pro666=
|
|
XM_011544807.1:c.1542G>C
|
XP_011543109.1:p.Pro514=
|
|
XM_011544808.1:c.1407G>C
|
XP_011543110.1:p.Pro469=
|
|
XM_005273824.4:c.2235G>C
|
XP_005273881.1:p.Pro745=
|
|
XM_005273826.4:c.1983G>C
|
XP_005273883.1:p.Pro661=
|
|
XM_005273830.4:c.1545G>C
|
XP_005273887.1:p.Pro515=
|
|
XM_005273831.4:c.1545G>C
|
XP_005273888.1:p.Pro515=
|
|
XM_005273832.4:c.1515G>C
|
XP_005273889.1:p.Pro505=
|
|
XM_011544802.3:c.1998G>C
|
XP_011543104.1:p.Pro666=
|
|
XM_011544807.3:c.1542G>C
|
XP_011543109.1:p.Pro514=
|
|
XM_011544808.3:c.1407G>C
|
XP_011543110.1:p.Pro469=
|
|
XM_017017328.2:c.2019G>C
|
XP_016872817.1:p.Pro673=
|
|
XM_017017329.2:c.2016G>C
|
XP_016872818.1:p.Pro672=
|
|
XM_017017330.2:c.1515G>C
|
XP_016872819.1:p.Pro505=
|
|
XM_017017331.2:c.1515G>C
|
XP_016872820.1:p.Pro505=
|
|
XM_017017332.2:c.1329G>C
|
XP_016872821.1:p.Pro443=
|
|
XM_017017333.2:c.1296G>C
|
XP_016872822.1:p.Pro432=
|
|
XM_017017334.2:c.1296G>C
|
XP_016872823.1:p.Pro432=
|
|
XM_017017335.2:c.1296G>C
|
XP_016872824.1:p.Pro432=
|
|
XM_017017336.2:c.1188G>C
|
XP_016872825.1:p.Pro396=
|
|
XM_024448392.1:c.2028G>C
|
XP_024304160.1:p.Pro676=
|
|
XM_024448393.1:c.1515G>C
|
XP_024304161.1:p.Pro505=
|
|
XR_001747789.2:n.2170G>C
|
|
|
XR_247191.3:n.2292G>C
|
|
|
NM_139075.4:c.2238G>C
MANE Select
|
NP_620714.2:p.Pro746=
|
|