ENST00000342992.11:c.52226C>A
(TTN)
|
ENSP00000343764.6:p.Pro17409His
|
|
ENST00000342175.11:c.33311C>A
(TTN)
|
ENSP00000340554.6:p.Pro11104His
|
|
ENST00000359218.10:c.33110C>A
(TTN)
|
ENSP00000352154.5:p.Pro11037His
|
|
ENST00000342175.10:c.33311C>A
(TTN)
|
ENSP00000340554.6:p.Pro11104His
|
|
ENST00000342992.10:c.52226C>A
(TTN)
|
ENSP00000343764.6:p.Pro17409His
|
|
ENST00000359218.9:c.33110C>A
(TTN)
|
ENSP00000352154.5:p.Pro11037His
|
|
ENST00000460472.6:c.32735C>A
(TTN)
|
ENSP00000434586.1:p.Pro10912His
|
|
ENST00000589042.5:c.59930C>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19977His
|
|
ENST00000591111.5:c.55007C>A
(TTN)
|
ENSP00000465570.1:p.Pro18336His
|
|
ENST00000615779.4:c.55007C>A
(TTN)
|
ENSP00000483597.1:p.Pro18336His
|
|
NM_001256850.1:c.55007C>A
(TTN)
|
NP_001243779.1:p.Pro18336His
|
|
NM_001267550.2:c.59930C>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19977His
|
|
NM_003319.4:c.32735C>A
(TTN)
|
NP_003310.4:p.Pro10912His
|
|
NM_133378.4:c.52226C>A
(TTN)
|
NP_596869.4:p.Pro17409His
|
|
NM_133432.3:c.33110C>A
(TTN)
|
NP_597676.3:p.Pro11037His
|
|
NM_133437.4:c.33311C>A
(TTN)
|
NP_597681.4:p.Pro11104His
|
|
NR_038271.1:n.597-5707G>T
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+575G>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.59027C>A
(TTN)
|
XP_011510031.1:p.Pro19676His
|
|
XM_011511730.1:c.32921C>A
(TTN)
|
XP_011510032.1:p.Pro10974His
|
|
XM_011511731.1:c.32780C>A
(TTN)
|
XP_011510033.1:p.Pro10927His
|
|
XM_017004819.1:c.58823C>A
(TTN)
|
XP_016860308.1:p.Pro19608His
|
|
XM_017004820.1:c.54221C>A
(TTN)
|
XP_016860309.1:p.Pro18074His
|
|
XM_017004821.1:c.54218C>A
(TTN)
|
XP_016860310.1:p.Pro18073His
|
|
XM_017004822.1:c.51260C>A
(TTN)
|
XP_016860311.1:p.Pro17087His
|
|
XM_017004823.1:c.32876C>A
(TTN)
|
XP_016860312.1:p.Pro10959His
|
|
XM_024453094.1:c.54371C>A
(TTN)
|
XP_024308862.1:p.Pro18124His
|
|
XM_024453095.1:c.54368C>A
(TTN)
|
XP_024308863.1:p.Pro18123His
|
|
XM_024453096.1:c.53801C>A
(TTN)
|
XP_024308864.1:p.Pro17934His
|
|
XM_024453097.1:c.51143C>A
(TTN)
|
XP_024308865.1:p.Pro17048His
|
|
XM_024453098.1:c.51062C>A
(TTN)
|
XP_024308866.1:p.Pro17021His
|
|
XM_024453099.1:c.32825C>A
(TTN)
|
XP_024308867.1:p.Pro10942His
|
|
XM_024453100.1:c.22679C>A
(TTN)
|
XP_024308868.1:p.Pro7560His
|
|