ENST00000342992.11:c.90418G>C
(TTN)
|
ENSP00000343764.6:p.Glu30140Gln
|
|
ENST00000342175.11:c.71503G>C
(TTN)
|
ENSP00000340554.6:p.Glu23835Gln
|
|
ENST00000359218.10:c.71302G>C
(TTN)
|
ENSP00000352154.5:p.Glu23768Gln
|
|
ENST00000342175.10:c.71503G>C
(TTN)
|
ENSP00000340554.6:p.Glu23835Gln
|
|
ENST00000342992.10:c.90418G>C
(TTN)
|
ENSP00000343764.6:p.Glu30140Gln
|
|
ENST00000359218.9:c.71302G>C
(TTN)
|
ENSP00000352154.5:p.Glu23768Gln
|
|
ENST00000460472.6:c.70927G>C
(TTN)
|
ENSP00000434586.1:p.Glu23643Gln
|
|
ENST00000589042.5:c.98122G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu32708Gln
|
|
ENST00000591111.5:c.93199G>C
(TTN)
|
ENSP00000465570.1:p.Glu31067Gln
|
|
ENST00000615779.4:c.93199G>C
(TTN)
|
ENSP00000483597.1:p.Glu31067Gln
|
|
NM_001256850.1:c.93199G>C
(TTN)
|
NP_001243779.1:p.Glu31067Gln
|
|
NM_001267550.2:c.98122G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu32708Gln
|
|
NM_003319.4:c.70927G>C
(TTN)
|
NP_003310.4:p.Glu23643Gln
|
|
NM_133378.4:c.90418G>C
(TTN)
|
NP_596869.4:p.Glu30140Gln
|
|
NM_133432.3:c.71302G>C
(TTN)
|
NP_597676.3:p.Glu23768Gln
|
|
NM_133437.4:c.71503G>C
(TTN)
|
NP_597681.4:p.Glu23835Gln
|
|
NR_038271.1:n.446+16307C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.1840+53C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.97219G>C
(TTN)
|
XP_011510031.1:p.Glu32407Gln
|
|
XM_011511730.1:c.71113G>C
(TTN)
|
XP_011510032.1:p.Glu23705Gln
|
|
XM_011511731.1:c.70972G>C
(TTN)
|
XP_011510033.1:p.Glu23658Gln
|
|
XM_017004819.1:c.97015G>C
(TTN)
|
XP_016860308.1:p.Glu32339Gln
|
|
XM_017004820.1:c.92413G>C
(TTN)
|
XP_016860309.1:p.Glu30805Gln
|
|
XM_017004821.1:c.92410G>C
(TTN)
|
XP_016860310.1:p.Glu30804Gln
|
|
XM_017004822.1:c.89452G>C
(TTN)
|
XP_016860311.1:p.Glu29818Gln
|
|
XM_017004823.1:c.71068G>C
(TTN)
|
XP_016860312.1:p.Glu23690Gln
|
|
XM_024453094.1:c.92563G>C
(TTN)
|
XP_024308862.1:p.Glu30855Gln
|
|
XM_024453095.1:c.92560G>C
(TTN)
|
XP_024308863.1:p.Glu30854Gln
|
|
XM_024453096.1:c.91993G>C
(TTN)
|
XP_024308864.1:p.Glu30665Gln
|
|
XM_024453097.1:c.89335G>C
(TTN)
|
XP_024308865.1:p.Glu29779Gln
|
|
XM_024453098.1:c.89254G>C
(TTN)
|
XP_024308866.1:p.Glu29752Gln
|
|
XM_024453099.1:c.71017G>C
(TTN)
|
XP_024308867.1:p.Glu23673Gln
|
|
XM_024453100.1:c.60871G>C
(TTN)
|
XP_024308868.1:p.Glu20291Gln
|
|