ENST00000342992.11:c.53107C>G
(TTN)
|
ENSP00000343764.6:p.Pro17703Ala
|
|
ENST00000342175.11:c.34192C>G
(TTN)
|
ENSP00000340554.6:p.Pro11398Ala
|
|
ENST00000359218.10:c.33991C>G
(TTN)
|
ENSP00000352154.5:p.Pro11331Ala
|
|
ENST00000342175.10:c.34192C>G
(TTN)
|
ENSP00000340554.6:p.Pro11398Ala
|
|
ENST00000342992.10:c.53107C>G
(TTN)
|
ENSP00000343764.6:p.Pro17703Ala
|
|
ENST00000359218.9:c.33991C>G
(TTN)
|
ENSP00000352154.5:p.Pro11331Ala
|
|
ENST00000460472.6:c.33616C>G
(TTN)
|
ENSP00000434586.1:p.Pro11206Ala
|
|
ENST00000589042.5:c.60811C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro20271Ala
|
|
ENST00000591111.5:c.55888C>G
(TTN)
|
ENSP00000465570.1:p.Pro18630Ala
|
|
ENST00000615779.4:c.55888C>G
(TTN)
|
ENSP00000483597.1:p.Pro18630Ala
|
|
NM_001256850.1:c.55888C>G
(TTN)
|
NP_001243779.1:p.Pro18630Ala
|
|
NM_001267550.2:c.60811C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro20271Ala
|
|
NM_003319.4:c.33616C>G
(TTN)
|
NP_003310.4:p.Pro11206Ala
|
|
NM_133378.4:c.53107C>G
(TTN)
|
NP_596869.4:p.Pro17703Ala
|
|
NM_133432.3:c.33991C>G
(TTN)
|
NP_597676.3:p.Pro11331Ala
|
|
NM_133437.4:c.34192C>G
(TTN)
|
NP_597681.4:p.Pro11398Ala
|
|
NR_038271.1:n.597-6682G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.3189-225G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.59908C>G
(TTN)
|
XP_011510031.1:p.Pro19970Ala
|
|
XM_011511730.1:c.33802C>G
(TTN)
|
XP_011510032.1:p.Pro11268Ala
|
|
XM_011511731.1:c.33661C>G
(TTN)
|
XP_011510033.1:p.Pro11221Ala
|
|
XM_017004819.1:c.59704C>G
(TTN)
|
XP_016860308.1:p.Pro19902Ala
|
|
XM_017004820.1:c.55102C>G
(TTN)
|
XP_016860309.1:p.Pro18368Ala
|
|
XM_017004821.1:c.55099C>G
(TTN)
|
XP_016860310.1:p.Pro18367Ala
|
|
XM_017004822.1:c.52141C>G
(TTN)
|
XP_016860311.1:p.Pro17381Ala
|
|
XM_017004823.1:c.33757C>G
(TTN)
|
XP_016860312.1:p.Pro11253Ala
|
|
XM_024453094.1:c.55252C>G
(TTN)
|
XP_024308862.1:p.Pro18418Ala
|
|
XM_024453095.1:c.55249C>G
(TTN)
|
XP_024308863.1:p.Pro18417Ala
|
|
XM_024453096.1:c.54682C>G
(TTN)
|
XP_024308864.1:p.Pro18228Ala
|
|
XM_024453097.1:c.52024C>G
(TTN)
|
XP_024308865.1:p.Pro17342Ala
|
|
XM_024453098.1:c.51943C>G
(TTN)
|
XP_024308866.1:p.Pro17315Ala
|
|
XM_024453099.1:c.33706C>G
(TTN)
|
XP_024308867.1:p.Pro11236Ala
|
|
XM_024453100.1:c.23560C>G
(TTN)
|
XP_024308868.1:p.Pro7854Ala
|
|