ENST00000342992.11:c.53109T>C
(TTN)
|
ENSP00000343764.6:p.Pro17703=
|
|
ENST00000342175.11:c.34194T>C
(TTN)
|
ENSP00000340554.6:p.Pro11398=
|
|
ENST00000359218.10:c.33993T>C
(TTN)
|
ENSP00000352154.5:p.Pro11331=
|
|
ENST00000342175.10:c.34194T>C
(TTN)
|
ENSP00000340554.6:p.Pro11398=
|
|
ENST00000342992.10:c.53109T>C
(TTN)
|
ENSP00000343764.6:p.Pro17703=
|
|
ENST00000359218.9:c.33993T>C
(TTN)
|
ENSP00000352154.5:p.Pro11331=
|
|
ENST00000460472.6:c.33618T>C
(TTN)
|
ENSP00000434586.1:p.Pro11206=
|
|
ENST00000589042.5:c.60813T>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro20271=
|
|
ENST00000591111.5:c.55890T>C
(TTN)
|
ENSP00000465570.1:p.Pro18630=
|
|
ENST00000615779.4:c.55890T>C
(TTN)
|
ENSP00000483597.1:p.Pro18630=
|
|
NM_001256850.1:c.55890T>C
(TTN)
|
NP_001243779.1:p.Pro18630=
|
|
NM_001267550.2:c.60813T>C
(TTN)
MANE Select
|
NP_001254479.2:p.Pro20271=
|
|
NM_003319.4:c.33618T>C
(TTN)
|
NP_003310.4:p.Pro11206=
|
|
NM_133378.4:c.53109T>C
(TTN)
|
NP_596869.4:p.Pro17703=
|
|
NM_133432.3:c.33993T>C
(TTN)
|
NP_597676.3:p.Pro11331=
|
|
NM_133437.4:c.34194T>C
(TTN)
|
NP_597681.4:p.Pro11398=
|
|
NR_038271.1:n.597-6684A>G
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-227A>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.59910T>C
(TTN)
|
XP_011510031.1:p.Pro19970=
|
|
XM_011511730.1:c.33804T>C
(TTN)
|
XP_011510032.1:p.Pro11268=
|
|
XM_011511731.1:c.33663T>C
(TTN)
|
XP_011510033.1:p.Pro11221=
|
|
XM_017004819.1:c.59706T>C
(TTN)
|
XP_016860308.1:p.Pro19902=
|
|
XM_017004820.1:c.55104T>C
(TTN)
|
XP_016860309.1:p.Pro18368=
|
|
XM_017004821.1:c.55101T>C
(TTN)
|
XP_016860310.1:p.Pro18367=
|
|
XM_017004822.1:c.52143T>C
(TTN)
|
XP_016860311.1:p.Pro17381=
|
|
XM_017004823.1:c.33759T>C
(TTN)
|
XP_016860312.1:p.Pro11253=
|
|
XM_024453094.1:c.55254T>C
(TTN)
|
XP_024308862.1:p.Pro18418=
|
|
XM_024453095.1:c.55251T>C
(TTN)
|
XP_024308863.1:p.Pro18417=
|
|
XM_024453096.1:c.54684T>C
(TTN)
|
XP_024308864.1:p.Pro18228=
|
|
XM_024453097.1:c.52026T>C
(TTN)
|
XP_024308865.1:p.Pro17342=
|
|
XM_024453098.1:c.51945T>C
(TTN)
|
XP_024308866.1:p.Pro17315=
|
|
XM_024453099.1:c.33708T>C
(TTN)
|
XP_024308867.1:p.Pro11236=
|
|
XM_024453100.1:c.23562T>C
(TTN)
|
XP_024308868.1:p.Pro7854=
|
|