ENST00000378154.3:c.2459T>C
|
ENSP00000367396.2:p.Val820Ala
|
|
ENST00000378158.6:c.2456T>C
|
ENSP00000367400.2:p.Val819Ala
|
|
ENST00000378163.7:c.2510T>C
MANE Select
|
ENSP00000367405.1:p.Val837Ala
|
|
ENST00000378166.9:c.2408T>C
|
ENSP00000367408.5:p.Val803Ala
|
|
ENST00000378168.8:c.2513T>C
|
ENSP00000367410.4:p.Val838Ala
|
|
ENST00000378179.9:c.1130T>C
|
ENSP00000367421.4:p.Val377Ala
|
|
ENST00000421587.8:c.2441T>C
|
ENSP00000400526.4:p.Val814Ala
|
|
ENST00000442742.7:c.2372T>C
|
ENSP00000398007.3:p.Val791Ala
|
|
ENST00000642499.1:n.1289T>C
|
|
|
ENST00000643733.1:c.282T>C
|
|
|
ENST00000644219.1:c.2492T>C
|
ENSP00000495357.1:p.Val831Ala
|
|
ENST00000644347.1:c.2423T>C
|
ENSP00000494183.1:p.Val808Ala
|
|
ENST00000645566.1:c.2495T>C
|
ENSP00000494788.1:p.Val832Ala
|
|
ENST00000645937.2:n.2741T>C
|
|
|
ENST00000645986.2:c.2477T>C
|
ENSP00000494409.2:p.Val826Ala
|
|
ENST00000646087.2:c.1832T>C
|
ENSP00000495510.2:p.Val611Ala
|
|
ENST00000646120.2:c.2426T>C
|
ENSP00000495291.2:p.Val809Ala
|
|
ENST00000675354.1:c.2444T>C
|
ENSP00000502315.1:p.Val815Ala
|
|
ENST00000378158.5:c.2459T>C
|
ENSP00000367400.1:p.Val820Ala
|
|
ENST00000378163.5:c.2510T>C
|
ENSP00000367405.1:p.Val837Ala
|
|
ENST00000378166.8:c.2495T>C
|
ENSP00000367408.4:p.Val832Ala
|
|
ENST00000378168.6:c.875T>C
|
ENSP00000367410.2:p.Val292Ala
|
|
ENST00000378179.7:c.1286T>C
|
ENSP00000367421.3:p.Val429Ala
|
|
ENST00000421587.6:c.2423T>C
|
ENSP00000400526.2:p.Val808Ala
|
|
ENST00000442742.6:c.2426T>C
|
ENSP00000398007.2:p.Val809Ala
|
|
NM_001126054.2:c.2426T>C
|
NP_001119526.1:p.Val809Ala
|
|
NM_001126055.2:c.2423T>C
|
NP_001119527.1:p.Val808Ala
|
|
NM_003688.3:c.2495T>C
|
NP_003679.2:p.Val832Ala
|
|
XM_005272686.3:c.2492T>C
|
XP_005272743.1:p.Val831Ala
|
|
XM_006724566.2:c.2387T>C
|
XP_006724629.1:p.Val796Ala
|
|
XM_011543993.1:c.2510T>C
|
XP_011542295.1:p.Val837Ala
|
|
XM_011543994.1:c.2474T>C
|
XP_011542296.1:p.Val825Ala
|
|
XM_011543995.1:c.2441T>C
|
XP_011542297.1:p.Val814Ala
|
|
XM_011543996.1:c.2405T>C
|
XP_011542298.1:p.Val802Ala
|
|
XM_011543997.1:c.1937T>C
|
XP_011542299.1:p.Val646Ala
|
|
XM_005272686.4:c.2492T>C
|
XP_005272743.1:p.Val831Ala
|
|
XM_006724566.3:c.2387T>C
|
XP_006724629.1:p.Val796Ala
|
|
XM_011543993.2:c.2510T>C
|
XP_011542295.1:p.Val837Ala
|
|
XM_011543994.2:c.2474T>C
|
XP_011542296.1:p.Val825Ala
|
|
XM_011543995.2:c.2441T>C
|
XP_011542297.1:p.Val814Ala
|
|
XM_011543996.2:c.2405T>C
|
XP_011542298.1:p.Val802Ala
|
|
XM_011543997.3:c.1937T>C
|
XP_011542299.1:p.Val646Ala
|
|
XM_024452473.1:c.1832T>C
|
XP_024308241.1:p.Val611Ala
|
|
NM_001367721.1:c.2510T>C
MANE Select
|
NP_001354650.1:p.Val837Ala
|
|