ENST00000342992.11:c.83345A>C
(TTN)
|
ENSP00000343764.6:p.Tyr27782Ser
|
|
ENST00000342175.11:c.64430A>C
(TTN)
|
ENSP00000340554.6:p.Tyr21477Ser
|
|
ENST00000359218.10:c.64229A>C
(TTN)
|
ENSP00000352154.5:p.Tyr21410Ser
|
|
ENST00000342175.10:c.64430A>C
(TTN)
|
ENSP00000340554.6:p.Tyr21477Ser
|
|
ENST00000342992.10:c.83345A>C
(TTN)
|
ENSP00000343764.6:p.Tyr27782Ser
|
|
ENST00000359218.9:c.64229A>C
(TTN)
|
ENSP00000352154.5:p.Tyr21410Ser
|
|
ENST00000460472.6:c.63854A>C
(TTN)
|
ENSP00000434586.1:p.Tyr21285Ser
|
|
ENST00000589042.5:c.91049A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Tyr30350Ser
|
|
ENST00000591111.5:c.86126A>C
(TTN)
|
ENSP00000465570.1:p.Tyr28709Ser
|
|
ENST00000615779.4:c.86126A>C
(TTN)
|
ENSP00000483597.1:p.Tyr28709Ser
|
|
NM_001256850.1:c.86126A>C
(TTN)
|
NP_001243779.1:p.Tyr28709Ser
|
|
NM_001267550.2:c.91049A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Tyr30350Ser
|
|
NM_003319.4:c.63854A>C
(TTN)
|
NP_003310.4:p.Tyr21285Ser
|
|
NM_133378.4:c.83345A>C
(TTN)
|
NP_596869.4:p.Tyr27782Ser
|
|
NM_133432.3:c.64229A>C
(TTN)
|
NP_597676.3:p.Tyr21410Ser
|
|
NM_133437.4:c.64430A>C
(TTN)
|
NP_597681.4:p.Tyr21477Ser
|
|
NR_038271.1:n.447-19449T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2043+9490T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.90146A>C
(TTN)
|
XP_011510031.1:p.Tyr30049Ser
|
|
XM_011511730.1:c.64040A>C
(TTN)
|
XP_011510032.1:p.Tyr21347Ser
|
|
XM_011511731.1:c.63899A>C
(TTN)
|
XP_011510033.1:p.Tyr21300Ser
|
|
XM_017004819.1:c.89942A>C
(TTN)
|
XP_016860308.1:p.Tyr29981Ser
|
|
XM_017004820.1:c.85340A>C
(TTN)
|
XP_016860309.1:p.Tyr28447Ser
|
|
XM_017004821.1:c.85337A>C
(TTN)
|
XP_016860310.1:p.Tyr28446Ser
|
|
XM_017004822.1:c.82379A>C
(TTN)
|
XP_016860311.1:p.Tyr27460Ser
|
|
XM_017004823.1:c.63995A>C
(TTN)
|
XP_016860312.1:p.Tyr21332Ser
|
|
XM_024453094.1:c.85490A>C
(TTN)
|
XP_024308862.1:p.Tyr28497Ser
|
|
XM_024453095.1:c.85487A>C
(TTN)
|
XP_024308863.1:p.Tyr28496Ser
|
|
XM_024453096.1:c.84920A>C
(TTN)
|
XP_024308864.1:p.Tyr28307Ser
|
|
XM_024453097.1:c.82262A>C
(TTN)
|
XP_024308865.1:p.Tyr27421Ser
|
|
XM_024453098.1:c.82181A>C
(TTN)
|
XP_024308866.1:p.Tyr27394Ser
|
|
XM_024453099.1:c.63944A>C
(TTN)
|
XP_024308867.1:p.Tyr21315Ser
|
|
XM_024453100.1:c.53798A>C
(TTN)
|
XP_024308868.1:p.Tyr17933Ser
|
|