ENST00000342992.11:c.91972C>G
(TTN)
|
ENSP00000343764.6:p.Pro30658Ala
|
|
ENST00000342175.11:c.73057C>G
(TTN)
|
ENSP00000340554.6:p.Pro24353Ala
|
|
ENST00000359218.10:c.72856C>G
(TTN)
|
ENSP00000352154.5:p.Pro24286Ala
|
|
ENST00000342175.10:c.73057C>G
(TTN)
|
ENSP00000340554.6:p.Pro24353Ala
|
|
ENST00000342992.10:c.91972C>G
(TTN)
|
ENSP00000343764.6:p.Pro30658Ala
|
|
ENST00000359218.9:c.72856C>G
(TTN)
|
ENSP00000352154.5:p.Pro24286Ala
|
|
ENST00000460472.6:c.72481C>G
(TTN)
|
ENSP00000434586.1:p.Pro24161Ala
|
|
ENST00000589042.5:c.99676C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Pro33226Ala
|
|
ENST00000591111.5:c.94753C>G
(TTN)
|
ENSP00000465570.1:p.Pro31585Ala
|
|
ENST00000615779.4:c.94753C>G
(TTN)
|
ENSP00000483597.1:p.Pro31585Ala
|
|
NM_001256850.1:c.94753C>G
(TTN)
|
NP_001243779.1:p.Pro31585Ala
|
|
NM_001267550.2:c.99676C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Pro33226Ala
|
|
NM_003319.4:c.72481C>G
(TTN)
|
NP_003310.4:p.Pro24161Ala
|
|
NM_133378.4:c.91972C>G
(TTN)
|
NP_596869.4:p.Pro30658Ala
|
|
NM_133432.3:c.72856C>G
(TTN)
|
NP_597676.3:p.Pro24286Ala
|
|
NM_133437.4:c.73057C>G
(TTN)
|
NP_597681.4:p.Pro24353Ala
|
|
NR_038271.1:n.446+13895G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.487G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.98773C>G
(TTN)
|
XP_011510031.1:p.Pro32925Ala
|
|
XM_011511730.1:c.72667C>G
(TTN)
|
XP_011510032.1:p.Pro24223Ala
|
|
XM_011511731.1:c.72526C>G
(TTN)
|
XP_011510033.1:p.Pro24176Ala
|
|
XM_017004819.1:c.98569C>G
(TTN)
|
XP_016860308.1:p.Pro32857Ala
|
|
XM_017004820.1:c.93967C>G
(TTN)
|
XP_016860309.1:p.Pro31323Ala
|
|
XM_017004821.1:c.93964C>G
(TTN)
|
XP_016860310.1:p.Pro31322Ala
|
|
XM_017004822.1:c.91006C>G
(TTN)
|
XP_016860311.1:p.Pro30336Ala
|
|
XM_017004823.1:c.72622C>G
(TTN)
|
XP_016860312.1:p.Pro24208Ala
|
|
XM_024453094.1:c.94117C>G
(TTN)
|
XP_024308862.1:p.Pro31373Ala
|
|
XM_024453095.1:c.94114C>G
(TTN)
|
XP_024308863.1:p.Pro31372Ala
|
|
XM_024453096.1:c.93547C>G
(TTN)
|
XP_024308864.1:p.Pro31183Ala
|
|
XM_024453097.1:c.90889C>G
(TTN)
|
XP_024308865.1:p.Pro30297Ala
|
|
XM_024453098.1:c.90808C>G
(TTN)
|
XP_024308866.1:p.Pro30270Ala
|
|
XM_024453099.1:c.72571C>G
(TTN)
|
XP_024308867.1:p.Pro24191Ala
|
|
XM_024453100.1:c.62425C>G
(TTN)
|
XP_024308868.1:p.Pro20809Ala
|
|