ENST00000342992.11:c.98342T>A
(TTN)
|
ENSP00000343764.6:p.Leu32781His
|
|
ENST00000342175.11:c.79427T>A
(TTN)
|
ENSP00000340554.6:p.Leu26476His
|
|
ENST00000359218.10:c.79226T>A
(TTN)
|
ENSP00000352154.5:p.Leu26409His
|
|
ENST00000342175.10:c.79427T>A
(TTN)
|
ENSP00000340554.6:p.Leu26476His
|
|
ENST00000342992.10:c.98342T>A
(TTN)
|
ENSP00000343764.6:p.Leu32781His
|
|
ENST00000359218.9:c.79226T>A
(TTN)
|
ENSP00000352154.5:p.Leu26409His
|
|
ENST00000460472.6:c.78851T>A
(TTN)
|
ENSP00000434586.1:p.Leu26284His
|
|
ENST00000589042.5:c.106046T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Leu35349His
|
|
ENST00000591111.5:c.101123T>A
(TTN)
|
ENSP00000465570.1:p.Leu33708His
|
|
ENST00000615779.4:c.101123T>A
(TTN)
|
ENSP00000483597.1:p.Leu33708His
|
|
NM_001256850.1:c.101123T>A
(TTN)
|
NP_001243779.1:p.Leu33708His
|
|
NM_001267550.2:c.106046T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Leu35349His
|
|
NM_003319.4:c.78851T>A
(TTN)
|
NP_003310.4:p.Leu26284His
|
|
NM_133378.4:c.98342T>A
(TTN)
|
NP_596869.4:p.Leu32781His
|
|
NM_133432.3:c.79226T>A
(TTN)
|
NP_597676.3:p.Leu26409His
|
|
NM_133437.4:c.79427T>A
(TTN)
|
NP_597681.4:p.Leu26476His
|
|
NR_038271.1:n.446+6933A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.220-5163A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.105143T>A
(TTN)
|
XP_011510031.1:p.Leu35048His
|
|
XM_011511730.1:c.79037T>A
(TTN)
|
XP_011510032.1:p.Leu26346His
|
|
XM_011511731.1:c.78896T>A
(TTN)
|
XP_011510033.1:p.Leu26299His
|
|
XM_017004819.1:c.104939T>A
(TTN)
|
XP_016860308.1:p.Leu34980His
|
|
XM_017004820.1:c.100337T>A
(TTN)
|
XP_016860309.1:p.Leu33446His
|
|
XM_017004821.1:c.100334T>A
(TTN)
|
XP_016860310.1:p.Leu33445His
|
|
XM_017004822.1:c.97376T>A
(TTN)
|
XP_016860311.1:p.Leu32459His
|
|
XM_017004823.1:c.78992T>A
(TTN)
|
XP_016860312.1:p.Leu26331His
|
|
XM_024453094.1:c.100487T>A
(TTN)
|
XP_024308862.1:p.Leu33496His
|
|
XM_024453095.1:c.100484T>A
(TTN)
|
XP_024308863.1:p.Leu33495His
|
|
XM_024453096.1:c.99917T>A
(TTN)
|
XP_024308864.1:p.Leu33306His
|
|
XM_024453097.1:c.97259T>A
(TTN)
|
XP_024308865.1:p.Leu32420His
|
|
XM_024453098.1:c.97178T>A
(TTN)
|
XP_024308866.1:p.Leu32393His
|
|
XM_024453099.1:c.78941T>A
(TTN)
|
XP_024308867.1:p.Leu26314His
|
|
XM_024453100.1:c.68795T>A
(TTN)
|
XP_024308868.1:p.Leu22932His
|
|