ENST00000342992.11:c.52225C>G
(TTN)
|
ENSP00000343764.6:p.Pro17409Ala
|
|
ENST00000342175.11:c.33310C>G
(TTN)
|
ENSP00000340554.6:p.Pro11104Ala
|
|
ENST00000359218.10:c.33109C>G
(TTN)
|
ENSP00000352154.5:p.Pro11037Ala
|
|
ENST00000342175.10:c.33310C>G
(TTN)
|
ENSP00000340554.6:p.Pro11104Ala
|
|
ENST00000342992.10:c.52225C>G
(TTN)
|
ENSP00000343764.6:p.Pro17409Ala
|
|
ENST00000359218.9:c.33109C>G
(TTN)
|
ENSP00000352154.5:p.Pro11037Ala
|
|
ENST00000460472.6:c.32734C>G
(TTN)
|
ENSP00000434586.1:p.Pro10912Ala
|
|
ENST00000589042.5:c.59929C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19977Ala
|
|
ENST00000591111.5:c.55006C>G
(TTN)
|
ENSP00000465570.1:p.Pro18336Ala
|
|
ENST00000615779.4:c.55006C>G
(TTN)
|
ENSP00000483597.1:p.Pro18336Ala
|
|
NM_001256850.1:c.55006C>G
(TTN)
|
NP_001243779.1:p.Pro18336Ala
|
|
NM_001267550.2:c.59929C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19977Ala
|
|
NM_003319.4:c.32734C>G
(TTN)
|
NP_003310.4:p.Pro10912Ala
|
|
NM_133378.4:c.52225C>G
(TTN)
|
NP_596869.4:p.Pro17409Ala
|
|
NM_133432.3:c.33109C>G
(TTN)
|
NP_597676.3:p.Pro11037Ala
|
|
NM_133437.4:c.33310C>G
(TTN)
|
NP_597681.4:p.Pro11104Ala
|
|
NR_038271.1:n.597-5706G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+576G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59026C>G
(TTN)
|
XP_011510031.1:p.Pro19676Ala
|
|
XM_011511730.1:c.32920C>G
(TTN)
|
XP_011510032.1:p.Pro10974Ala
|
|
XM_011511731.1:c.32779C>G
(TTN)
|
XP_011510033.1:p.Pro10927Ala
|
|
XM_017004819.1:c.58822C>G
(TTN)
|
XP_016860308.1:p.Pro19608Ala
|
|
XM_017004820.1:c.54220C>G
(TTN)
|
XP_016860309.1:p.Pro18074Ala
|
|
XM_017004821.1:c.54217C>G
(TTN)
|
XP_016860310.1:p.Pro18073Ala
|
|
XM_017004822.1:c.51259C>G
(TTN)
|
XP_016860311.1:p.Pro17087Ala
|
|
XM_017004823.1:c.32875C>G
(TTN)
|
XP_016860312.1:p.Pro10959Ala
|
|
XM_024453094.1:c.54370C>G
(TTN)
|
XP_024308862.1:p.Pro18124Ala
|
|
XM_024453095.1:c.54367C>G
(TTN)
|
XP_024308863.1:p.Pro18123Ala
|
|
XM_024453096.1:c.53800C>G
(TTN)
|
XP_024308864.1:p.Pro17934Ala
|
|
XM_024453097.1:c.51142C>G
(TTN)
|
XP_024308865.1:p.Pro17048Ala
|
|
XM_024453098.1:c.51061C>G
(TTN)
|
XP_024308866.1:p.Pro17021Ala
|
|
XM_024453099.1:c.32824C>G
(TTN)
|
XP_024308867.1:p.Pro10942Ala
|
|
XM_024453100.1:c.22678C>G
(TTN)
|
XP_024308868.1:p.Pro7560Ala
|
|