ENST00000342992.11:c.67869A>C
(TTN)
|
ENSP00000343764.6:p.Gly22623=
|
|
ENST00000342175.11:c.48954A>C
(TTN)
|
ENSP00000340554.6:p.Gly16318=
|
|
ENST00000359218.10:c.48753A>C
(TTN)
|
ENSP00000352154.5:p.Gly16251=
|
|
ENST00000342175.10:c.48954A>C
(TTN)
|
ENSP00000340554.6:p.Gly16318=
|
|
ENST00000342992.10:c.67869A>C
(TTN)
|
ENSP00000343764.6:p.Gly22623=
|
|
ENST00000359218.9:c.48753A>C
(TTN)
|
ENSP00000352154.5:p.Gly16251=
|
|
ENST00000460472.6:c.48378A>C
(TTN)
|
ENSP00000434586.1:p.Gly16126=
|
|
ENST00000589042.5:c.75573A>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Gly25191=
|
|
ENST00000591111.5:c.70650A>C
(TTN)
|
ENSP00000465570.1:p.Gly23550=
|
|
ENST00000615779.4:c.70650A>C
(TTN)
|
ENSP00000483597.1:p.Gly23550=
|
|
NM_001256850.1:c.70650A>C
(TTN)
|
NP_001243779.1:p.Gly23550=
|
|
NM_001267550.2:c.75573A>C
(TTN)
MANE Select
|
NP_001254479.2:p.Gly25191=
|
|
NM_003319.4:c.48378A>C
(TTN)
|
NP_003310.4:p.Gly16126=
|
|
NM_133378.4:c.67869A>C
(TTN)
|
NP_596869.4:p.Gly22623=
|
|
NM_133432.3:c.48753A>C
(TTN)
|
NP_597676.3:p.Gly16251=
|
|
NM_133437.4:c.48954A>C
(TTN)
|
NP_597681.4:p.Gly16318=
|
|
NR_038271.1:n.447-741T>G
(TTN-AS1)
|
|
|
NR_038272.1:n.2044-12013T>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.74670A>C
(TTN)
|
XP_011510031.1:p.Gly24890=
|
|
XM_011511730.1:c.48564A>C
(TTN)
|
XP_011510032.1:p.Gly16188=
|
|
XM_011511731.1:c.48423A>C
(TTN)
|
XP_011510033.1:p.Gly16141=
|
|
XM_017004819.1:c.74466A>C
(TTN)
|
XP_016860308.1:p.Gly24822=
|
|
XM_017004820.1:c.69864A>C
(TTN)
|
XP_016860309.1:p.Gly23288=
|
|
XM_017004821.1:c.69861A>C
(TTN)
|
XP_016860310.1:p.Gly23287=
|
|
XM_017004822.1:c.66903A>C
(TTN)
|
XP_016860311.1:p.Gly22301=
|
|
XM_017004823.1:c.48519A>C
(TTN)
|
XP_016860312.1:p.Gly16173=
|
|
XM_024453094.1:c.70014A>C
(TTN)
|
XP_024308862.1:p.Gly23338=
|
|
XM_024453095.1:c.70011A>C
(TTN)
|
XP_024308863.1:p.Gly23337=
|
|
XM_024453096.1:c.69444A>C
(TTN)
|
XP_024308864.1:p.Gly23148=
|
|
XM_024453097.1:c.66786A>C
(TTN)
|
XP_024308865.1:p.Gly22262=
|
|
XM_024453098.1:c.66705A>C
(TTN)
|
XP_024308866.1:p.Gly22235=
|
|
XM_024453099.1:c.48468A>C
(TTN)
|
XP_024308867.1:p.Gly16156=
|
|
XM_024453100.1:c.38322A>C
(TTN)
|
XP_024308868.1:p.Gly12774=
|
|