ENST00000342992.11:c.57276T>A
(TTN)
|
ENSP00000343764.6:p.Pro19092=
|
|
ENST00000342175.11:c.38361T>A
(TTN)
|
ENSP00000340554.6:p.Pro12787=
|
|
ENST00000359218.10:c.38160T>A
(TTN)
|
ENSP00000352154.5:p.Pro12720=
|
|
ENST00000342175.10:c.38361T>A
(TTN)
|
ENSP00000340554.6:p.Pro12787=
|
|
ENST00000342992.10:c.57276T>A
(TTN)
|
ENSP00000343764.6:p.Pro19092=
|
|
ENST00000359218.9:c.38160T>A
(TTN)
|
ENSP00000352154.5:p.Pro12720=
|
|
ENST00000460472.6:c.37785T>A
(TTN)
|
ENSP00000434586.1:p.Pro12595=
|
|
ENST00000589042.5:c.64980T>A
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro21660=
|
|
ENST00000591111.5:c.60057T>A
(TTN)
|
ENSP00000465570.1:p.Pro20019=
|
|
ENST00000615779.4:c.60057T>A
(TTN)
|
ENSP00000483597.1:p.Pro20019=
|
|
NM_001256850.1:c.60057T>A
(TTN)
|
NP_001243779.1:p.Pro20019=
|
|
NM_001267550.2:c.64980T>A
(TTN)
MANE Select
|
NP_001254479.2:p.Pro21660=
|
|
NM_003319.4:c.37785T>A
(TTN)
|
NP_003310.4:p.Pro12595=
|
|
NM_133378.4:c.57276T>A
(TTN)
|
NP_596869.4:p.Pro19092=
|
|
NM_133432.3:c.38160T>A
(TTN)
|
NP_597676.3:p.Pro12720=
|
|
NM_133437.4:c.38361T>A
(TTN)
|
NP_597681.4:p.Pro12787=
|
|
NR_038271.1:n.597-13025A>T
(TTN-AS1)
|
|
|
NR_038272.1:n.2768-2A>T
(TTN-AS1)
|
|
|
XM_011511729.1:c.64077T>A
(TTN)
|
XP_011510031.1:p.Pro21359=
|
|
XM_011511730.1:c.37971T>A
(TTN)
|
XP_011510032.1:p.Pro12657=
|
|
XM_011511731.1:c.37830T>A
(TTN)
|
XP_011510033.1:p.Pro12610=
|
|
XM_017004819.1:c.63873T>A
(TTN)
|
XP_016860308.1:p.Pro21291=
|
|
XM_017004820.1:c.59271T>A
(TTN)
|
XP_016860309.1:p.Pro19757=
|
|
XM_017004821.1:c.59268T>A
(TTN)
|
XP_016860310.1:p.Pro19756=
|
|
XM_017004822.1:c.56310T>A
(TTN)
|
XP_016860311.1:p.Pro18770=
|
|
XM_017004823.1:c.37926T>A
(TTN)
|
XP_016860312.1:p.Pro12642=
|
|
XM_024453094.1:c.59421T>A
(TTN)
|
XP_024308862.1:p.Pro19807=
|
|
XM_024453095.1:c.59418T>A
(TTN)
|
XP_024308863.1:p.Pro19806=
|
|
XM_024453096.1:c.58851T>A
(TTN)
|
XP_024308864.1:p.Pro19617=
|
|
XM_024453097.1:c.56193T>A
(TTN)
|
XP_024308865.1:p.Pro18731=
|
|
XM_024453098.1:c.56112T>A
(TTN)
|
XP_024308866.1:p.Pro18704=
|
|
XM_024453099.1:c.37875T>A
(TTN)
|
XP_024308867.1:p.Pro12625=
|
|
XM_024453100.1:c.27729T>A
(TTN)
|
XP_024308868.1:p.Pro9243=
|
|