ENST00000342992.11:c.90394G>T
(TTN)
|
ENSP00000343764.6:p.Glu30132Ter
|
|
ENST00000342175.11:c.71479G>T
(TTN)
|
ENSP00000340554.6:p.Glu23827Ter
|
|
ENST00000359218.10:c.71278G>T
(TTN)
|
ENSP00000352154.5:p.Glu23760Ter
|
|
ENST00000342175.10:c.71479G>T
(TTN)
|
ENSP00000340554.6:p.Glu23827Ter
|
|
ENST00000342992.10:c.90394G>T
(TTN)
|
ENSP00000343764.6:p.Glu30132Ter
|
|
ENST00000359218.9:c.71278G>T
(TTN)
|
ENSP00000352154.5:p.Glu23760Ter
|
|
ENST00000460472.6:c.70903G>T
(TTN)
|
ENSP00000434586.1:p.Glu23635Ter
|
|
ENST00000589042.5:c.98098G>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32700Ter
|
|
ENST00000591111.5:c.93175G>T
(TTN)
|
ENSP00000465570.1:p.Glu31059Ter
|
|
ENST00000615779.4:c.93175G>T
(TTN)
|
ENSP00000483597.1:p.Glu31059Ter
|
|
NM_001256850.1:c.93175G>T
(TTN)
|
NP_001243779.1:p.Glu31059Ter
|
|
NM_001267550.2:c.98098G>T
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32700Ter
|
|
NM_003319.4:c.70903G>T
(TTN)
|
NP_003310.4:p.Glu23635Ter
|
|
NM_133378.4:c.90394G>T
(TTN)
|
NP_596869.4:p.Glu30132Ter
|
|
NM_133432.3:c.71278G>T
(TTN)
|
NP_597676.3:p.Glu23760Ter
|
|
NM_133437.4:c.71479G>T
(TTN)
|
NP_597681.4:p.Glu23827Ter
|
|
NR_038271.1:n.446+16432C>A
(TTN-AS1)
|
|
|
NR_038272.1:n.1841-39C>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.97195G>T
(TTN)
|
XP_011510031.1:p.Glu32399Ter
|
|
XM_011511730.1:c.71089G>T
(TTN)
|
XP_011510032.1:p.Glu23697Ter
|
|
XM_011511731.1:c.70948G>T
(TTN)
|
XP_011510033.1:p.Glu23650Ter
|
|
XM_017004819.1:c.96991G>T
(TTN)
|
XP_016860308.1:p.Glu32331Ter
|
|
XM_017004820.1:c.92389G>T
(TTN)
|
XP_016860309.1:p.Glu30797Ter
|
|
XM_017004821.1:c.92386G>T
(TTN)
|
XP_016860310.1:p.Glu30796Ter
|
|
XM_017004822.1:c.89428G>T
(TTN)
|
XP_016860311.1:p.Glu29810Ter
|
|
XM_017004823.1:c.71044G>T
(TTN)
|
XP_016860312.1:p.Glu23682Ter
|
|
XM_024453094.1:c.92539G>T
(TTN)
|
XP_024308862.1:p.Glu30847Ter
|
|
XM_024453095.1:c.92536G>T
(TTN)
|
XP_024308863.1:p.Glu30846Ter
|
|
XM_024453096.1:c.91969G>T
(TTN)
|
XP_024308864.1:p.Glu30657Ter
|
|
XM_024453097.1:c.89311G>T
(TTN)
|
XP_024308865.1:p.Glu29771Ter
|
|
XM_024453098.1:c.89230G>T
(TTN)
|
XP_024308866.1:p.Glu29744Ter
|
|
XM_024453099.1:c.70993G>T
(TTN)
|
XP_024308867.1:p.Glu23665Ter
|
|
XM_024453100.1:c.60847G>T
(TTN)
|
XP_024308868.1:p.Glu20283Ter
|
|