ENST00000342992.11:c.100160C>G
(TTN)
|
ENSP00000343764.6:p.Thr33387Ser
|
|
ENST00000342175.11:c.81245C>G
(TTN)
|
ENSP00000340554.6:p.Thr27082Ser
|
|
ENST00000359218.10:c.81044C>G
(TTN)
|
ENSP00000352154.5:p.Thr27015Ser
|
|
ENST00000342175.10:c.81245C>G
(TTN)
|
ENSP00000340554.6:p.Thr27082Ser
|
|
ENST00000342992.10:c.100160C>G
(TTN)
|
ENSP00000343764.6:p.Thr33387Ser
|
|
ENST00000359218.9:c.81044C>G
(TTN)
|
ENSP00000352154.5:p.Thr27015Ser
|
|
ENST00000460472.6:c.80669C>G
(TTN)
|
ENSP00000434586.1:p.Thr26890Ser
|
|
ENST00000589042.5:c.107864C>G
(TTN)
MANE Select
|
ENSP00000467141.1:p.Thr35955Ser
|
|
ENST00000591111.5:c.102941C>G
(TTN)
|
ENSP00000465570.1:p.Thr34314Ser
|
|
ENST00000615779.4:c.102941C>G
(TTN)
|
ENSP00000483597.1:p.Thr34314Ser
|
|
NM_001256850.1:c.102941C>G
(TTN)
|
NP_001243779.1:p.Thr34314Ser
|
|
NM_001267550.2:c.107864C>G
(TTN)
MANE Select
|
NP_001254479.2:p.Thr35955Ser
|
|
NM_003319.4:c.80669C>G
(TTN)
|
NP_003310.4:p.Thr26890Ser
|
|
NM_133378.4:c.100160C>G
(TTN)
|
NP_596869.4:p.Thr33387Ser
|
|
NM_133432.3:c.81044C>G
(TTN)
|
NP_597676.3:p.Thr27015Ser
|
|
NM_133437.4:c.81245C>G
(TTN)
|
NP_597681.4:p.Thr27082Ser
|
|
NR_038271.1:n.446+3488G>C
(TTN-AS1)
|
|
|
NR_038272.1:n.219+3488G>C
(TTN-AS1)
|
|
|
XM_011511729.1:c.106961C>G
(TTN)
|
XP_011510031.1:p.Thr35654Ser
|
|
XM_011511730.1:c.80855C>G
(TTN)
|
XP_011510032.1:p.Thr26952Ser
|
|
XM_011511731.1:c.80714C>G
(TTN)
|
XP_011510033.1:p.Thr26905Ser
|
|
XM_017004819.1:c.106757C>G
(TTN)
|
XP_016860308.1:p.Thr35586Ser
|
|
XM_017004820.1:c.102155C>G
(TTN)
|
XP_016860309.1:p.Thr34052Ser
|
|
XM_017004821.1:c.102152C>G
(TTN)
|
XP_016860310.1:p.Thr34051Ser
|
|
XM_017004822.1:c.99194C>G
(TTN)
|
XP_016860311.1:p.Thr33065Ser
|
|
XM_017004823.1:c.80810C>G
(TTN)
|
XP_016860312.1:p.Thr26937Ser
|
|
XM_024453094.1:c.102305C>G
(TTN)
|
XP_024308862.1:p.Thr34102Ser
|
|
XM_024453095.1:c.102302C>G
(TTN)
|
XP_024308863.1:p.Thr34101Ser
|
|
XM_024453096.1:c.101735C>G
(TTN)
|
XP_024308864.1:p.Thr33912Ser
|
|
XM_024453097.1:c.99077C>G
(TTN)
|
XP_024308865.1:p.Thr33026Ser
|
|
XM_024453098.1:c.98996C>G
(TTN)
|
XP_024308866.1:p.Thr32999Ser
|
|
XM_024453099.1:c.80759C>G
(TTN)
|
XP_024308867.1:p.Thr26920Ser
|
|
XM_024453100.1:c.70613C>G
(TTN)
|
XP_024308868.1:p.Thr23538Ser
|
|