ENST00000342992.11:c.90383C>G
(TTN)
|
ENSP00000343764.6:p.Thr30128Ser
|
|
ENST00000342175.11:c.71468C>G
(TTN)
|
ENSP00000340554.6:p.Thr23823Ser
|
|
ENST00000359218.10:c.71267C>G
(TTN)
|
ENSP00000352154.5:p.Thr23756Ser
|
|
ENST00000342175.10:c.71468C>G
(TTN)
|
ENSP00000340554.6:p.Thr23823Ser
|
|
ENST00000342992.10:c.90383C>G
(TTN)
|
ENSP00000343764.6:p.Thr30128Ser
|
|
ENST00000359218.9:c.71267C>G
(TTN)
|
ENSP00000352154.5:p.Thr23756Ser
|
|
ENST00000460472.6:c.70892C>G
(TTN)
|
ENSP00000434586.1:p.Thr23631Ser
|
|
ENST00000589042.5:c.98087C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr32696Ser
|
|
ENST00000591111.5:c.93164C>G
(TTN)
|
ENSP00000465570.1:p.Thr31055Ser
|
|
ENST00000615779.4:c.93164C>G
(TTN)
|
ENSP00000483597.1:p.Thr31055Ser
|
|
NM_001256850.1:c.93164C>G
(TTN)
|
NP_001243779.1:p.Thr31055Ser
|
|
NM_001267550.2:c.98087C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr32696Ser
|
|
NM_003319.4:c.70892C>G
(TTN)
|
NP_003310.4:p.Thr23631Ser
|
|
NM_133378.4:c.90383C>G
(TTN)
|
NP_596869.4:p.Thr30128Ser
|
|
NM_133432.3:c.71267C>G
(TTN)
|
NP_597676.3:p.Thr23756Ser
|
|
NM_133437.4:c.71468C>G
(TTN)
|
NP_597681.4:p.Thr23823Ser
|
|
NR_038271.1:n.446+16443G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-28G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.97184C>G
(TTN)
|
XP_011510031.1:p.Thr32395Ser
|
|
XM_011511730.1:c.71078C>G
(TTN)
|
XP_011510032.1:p.Thr23693Ser
|
|
XM_011511731.1:c.70937C>G
(TTN)
|
XP_011510033.1:p.Thr23646Ser
|
|
XM_017004819.1:c.96980C>G
(TTN)
|
XP_016860308.1:p.Thr32327Ser
|
|
XM_017004820.1:c.92378C>G
(TTN)
|
XP_016860309.1:p.Thr30793Ser
|
|
XM_017004821.1:c.92375C>G
(TTN)
|
XP_016860310.1:p.Thr30792Ser
|
|
XM_017004822.1:c.89417C>G
(TTN)
|
XP_016860311.1:p.Thr29806Ser
|
|
XM_017004823.1:c.71033C>G
(TTN)
|
XP_016860312.1:p.Thr23678Ser
|
|
XM_024453094.1:c.92528C>G
(TTN)
|
XP_024308862.1:p.Thr30843Ser
|
|
XM_024453095.1:c.92525C>G
(TTN)
|
XP_024308863.1:p.Thr30842Ser
|
|
XM_024453096.1:c.91958C>G
(TTN)
|
XP_024308864.1:p.Thr30653Ser
|
|
XM_024453097.1:c.89300C>G
(TTN)
|
XP_024308865.1:p.Thr29767Ser
|
|
XM_024453098.1:c.89219C>G
(TTN)
|
XP_024308866.1:p.Thr29740Ser
|
|
XM_024453099.1:c.70982C>G
(TTN)
|
XP_024308867.1:p.Thr23661Ser
|
|
XM_024453100.1:c.60836C>G
(TTN)
|
XP_024308868.1:p.Thr20279Ser
|
|