ENST00000342992.11:c.82638T>C
(TTN)
|
ENSP00000343764.6:p.Pro27546=
|
|
ENST00000342175.11:c.63723T>C
(TTN)
|
ENSP00000340554.6:p.Pro21241=
|
|
ENST00000359218.10:c.63522T>C
(TTN)
|
ENSP00000352154.5:p.Pro21174=
|
|
ENST00000342175.10:c.63723T>C
(TTN)
|
ENSP00000340554.6:p.Pro21241=
|
|
ENST00000342992.10:c.82638T>C
(TTN)
|
ENSP00000343764.6:p.Pro27546=
|
|
ENST00000359218.9:c.63522T>C
(TTN)
|
ENSP00000352154.5:p.Pro21174=
|
|
ENST00000460472.6:c.63147T>C
(TTN)
|
ENSP00000434586.1:p.Pro21049=
|
|
ENST00000589042.5:c.90342T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro30114=
|
|
ENST00000591111.5:c.85419T>C
(TTN)
|
ENSP00000465570.1:p.Pro28473=
|
|
ENST00000615779.4:c.85419T>C
(TTN)
|
ENSP00000483597.1:p.Pro28473=
|
|
NM_001256850.1:c.85419T>C
(TTN)
|
NP_001243779.1:p.Pro28473=
|
|
NM_001267550.2:c.90342T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Pro30114=
|
|
NM_003319.4:c.63147T>C
(TTN)
|
NP_003310.4:p.Pro21049=
|
|
NM_133378.4:c.82638T>C
(TTN)
|
NP_596869.4:p.Pro27546=
|
|
NM_133432.3:c.63522T>C
(TTN)
|
NP_597676.3:p.Pro21174=
|
|
NM_133437.4:c.63723T>C
(TTN)
|
NP_597681.4:p.Pro21241=
|
|
NR_038271.1:n.447-18742A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+10197A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.89439T>C
(TTN)
|
XP_011510031.1:p.Pro29813=
|
|
XM_011511730.1:c.63333T>C
(TTN)
|
XP_011510032.1:p.Pro21111=
|
|
XM_011511731.1:c.63192T>C
(TTN)
|
XP_011510033.1:p.Pro21064=
|
|
XM_017004819.1:c.89235T>C
(TTN)
|
XP_016860308.1:p.Pro29745=
|
|
XM_017004820.1:c.84633T>C
(TTN)
|
XP_016860309.1:p.Pro28211=
|
|
XM_017004821.1:c.84630T>C
(TTN)
|
XP_016860310.1:p.Pro28210=
|
|
XM_017004822.1:c.81672T>C
(TTN)
|
XP_016860311.1:p.Pro27224=
|
|
XM_017004823.1:c.63288T>C
(TTN)
|
XP_016860312.1:p.Pro21096=
|
|
XM_024453094.1:c.84783T>C
(TTN)
|
XP_024308862.1:p.Pro28261=
|
|
XM_024453095.1:c.84780T>C
(TTN)
|
XP_024308863.1:p.Pro28260=
|
|
XM_024453096.1:c.84213T>C
(TTN)
|
XP_024308864.1:p.Pro28071=
|
|
XM_024453097.1:c.81555T>C
(TTN)
|
XP_024308865.1:p.Pro27185=
|
|
XM_024453098.1:c.81474T>C
(TTN)
|
XP_024308866.1:p.Pro27158=
|
|
XM_024453099.1:c.63237T>C
(TTN)
|
XP_024308867.1:p.Pro21079=
|
|
XM_024453100.1:c.53091T>C
(TTN)
|
XP_024308868.1:p.Pro17697=
|
|