ENST00000342992.11:c.52227C>T
(TTN)
|
ENSP00000343764.6:p.Pro17409=
|
|
ENST00000342175.11:c.33312C>T
(TTN)
|
ENSP00000340554.6:p.Pro11104=
|
|
ENST00000359218.10:c.33111C>T
(TTN)
|
ENSP00000352154.5:p.Pro11037=
|
|
ENST00000342175.10:c.33312C>T
(TTN)
|
ENSP00000340554.6:p.Pro11104=
|
|
ENST00000342992.10:c.52227C>T
(TTN)
|
ENSP00000343764.6:p.Pro17409=
|
|
ENST00000359218.9:c.33111C>T
(TTN)
|
ENSP00000352154.5:p.Pro11037=
|
|
ENST00000460472.6:c.32736C>T
(TTN)
|
ENSP00000434586.1:p.Pro10912=
|
|
ENST00000589042.5:c.59931C>T
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro19977=
|
|
ENST00000591111.5:c.55008C>T
(TTN)
|
ENSP00000465570.1:p.Pro18336=
|
|
ENST00000615779.4:c.55008C>T
(TTN)
|
ENSP00000483597.1:p.Pro18336=
|
|
NM_001256850.1:c.55008C>T
(TTN)
|
NP_001243779.1:p.Pro18336=
|
|
NM_001267550.2:c.59931C>T
(TTN)
MANE Select
|
NP_001254479.2:p.Pro19977=
|
|
NM_003319.4:c.32736C>T
(TTN)
|
NP_003310.4:p.Pro10912=
|
|
NM_133378.4:c.52227C>T
(TTN)
|
NP_596869.4:p.Pro17409=
|
|
NM_133432.3:c.33111C>T
(TTN)
|
NP_597676.3:p.Pro11037=
|
|
NM_133437.4:c.33312C>T
(TTN)
|
NP_597681.4:p.Pro11104=
|
|
NR_038271.1:n.597-5708G>A
(TTN-AS1)
|
|
|
NR_038272.1:n.3364+574G>A
(TTN-AS1)
|
|
|
XM_011511729.1:c.59028C>T
(TTN)
|
XP_011510031.1:p.Pro19676=
|
|
XM_011511730.1:c.32922C>T
(TTN)
|
XP_011510032.1:p.Pro10974=
|
|
XM_011511731.1:c.32781C>T
(TTN)
|
XP_011510033.1:p.Pro10927=
|
|
XM_017004819.1:c.58824C>T
(TTN)
|
XP_016860308.1:p.Pro19608=
|
|
XM_017004820.1:c.54222C>T
(TTN)
|
XP_016860309.1:p.Pro18074=
|
|
XM_017004821.1:c.54219C>T
(TTN)
|
XP_016860310.1:p.Pro18073=
|
|
XM_017004822.1:c.51261C>T
(TTN)
|
XP_016860311.1:p.Pro17087=
|
|
XM_017004823.1:c.32877C>T
(TTN)
|
XP_016860312.1:p.Pro10959=
|
|
XM_024453094.1:c.54372C>T
(TTN)
|
XP_024308862.1:p.Pro18124=
|
|
XM_024453095.1:c.54369C>T
(TTN)
|
XP_024308863.1:p.Pro18123=
|
|
XM_024453096.1:c.53802C>T
(TTN)
|
XP_024308864.1:p.Pro17934=
|
|
XM_024453097.1:c.51144C>T
(TTN)
|
XP_024308865.1:p.Pro17048=
|
|
XM_024453098.1:c.51063C>T
(TTN)
|
XP_024308866.1:p.Pro17021=
|
|
XM_024453099.1:c.32826C>T
(TTN)
|
XP_024308867.1:p.Pro10942=
|
|
XM_024453100.1:c.22680C>T
(TTN)
|
XP_024308868.1:p.Pro7560=
|
|