ENST00000378154.3:c.2690G>T
|
ENSP00000367396.2:p.Cys897Phe
|
|
ENST00000378158.6:c.2687G>T
|
ENSP00000367400.2:p.Cys896Phe
|
|
ENST00000378163.7:c.2741G>T
MANE Select
|
ENSP00000367405.1:p.Cys914Phe
|
|
ENST00000378166.9:c.2639G>T
|
ENSP00000367408.5:p.Cys880Phe
|
|
ENST00000378168.8:c.2744G>T
|
ENSP00000367410.4:p.Cys915Phe
|
|
ENST00000378179.9:c.1361G>T
|
ENSP00000367421.4:p.Cys454Phe
|
|
ENST00000421587.8:c.2672G>T
|
ENSP00000400526.4:p.Cys891Phe
|
|
ENST00000442742.7:c.2603G>T
|
ENSP00000398007.3:p.Cys868Phe
|
|
ENST00000642499.1:n.1520G>T
|
|
|
ENST00000642641.1:n.900G>T
|
|
|
ENST00000643733.1:c.540G>T
|
|
|
ENST00000644219.1:c.2723G>T
|
ENSP00000495357.1:p.Cys908Phe
|
|
ENST00000644347.1:c.2654G>T
|
ENSP00000494183.1:p.Cys885Phe
|
|
ENST00000645566.1:c.2726G>T
|
ENSP00000494788.1:p.Cys909Phe
|
|
ENST00000645937.2:n.2972G>T
|
|
|
ENST00000645986.2:c.2828G>T
|
ENSP00000494409.2:p.Cys943Phe
|
|
ENST00000646087.2:c.2063G>T
|
ENSP00000495510.2:p.Cys688Phe
|
|
ENST00000646120.2:c.2657G>T
|
ENSP00000495291.2:p.Cys886Phe
|
|
ENST00000675354.1:c.2675G>T
|
ENSP00000502315.1:p.Cys892Phe
|
|
ENST00000378158.5:c.2690G>T
|
ENSP00000367400.1:p.Cys897Phe
|
|
ENST00000378163.5:c.2741G>T
|
ENSP00000367405.1:p.Cys914Phe
|
|
ENST00000378166.8:c.2726G>T
|
ENSP00000367408.4:p.Cys909Phe
|
|
ENST00000378168.6:c.1106G>T
|
ENSP00000367410.2:p.Cys369Phe
|
|
ENST00000378179.7:c.1517G>T
|
ENSP00000367421.3:p.Cys506Phe
|
|
ENST00000421587.6:c.2654G>T
|
ENSP00000400526.2:p.Cys885Phe
|
|
ENST00000442742.6:c.2657G>T
|
ENSP00000398007.2:p.Cys886Phe
|
|
NM_001126054.2:c.2657G>T
|
NP_001119526.1:p.Cys886Phe
|
|
NM_001126055.2:c.2654G>T
|
NP_001119527.1:p.Cys885Phe
|
|
NM_003688.3:c.2726G>T
|
NP_003679.2:p.Cys909Phe
|
|
XM_005272686.3:c.2723G>T
|
XP_005272743.1:p.Cys908Phe
|
|
XM_006724566.2:c.2618G>T
|
XP_006724629.1:p.Cys873Phe
|
|
XM_011543993.1:c.2741G>T
|
XP_011542295.1:p.Cys914Phe
|
|
XM_011543994.1:c.2705G>T
|
XP_011542296.1:p.Cys902Phe
|
|
XM_011543995.1:c.2672G>T
|
XP_011542297.1:p.Cys891Phe
|
|
XM_011543996.1:c.2636G>T
|
XP_011542298.1:p.Cys879Phe
|
|
XM_011543997.1:c.2168G>T
|
XP_011542299.1:p.Cys723Phe
|
|
XM_005272686.4:c.2723G>T
|
XP_005272743.1:p.Cys908Phe
|
|
XM_006724566.3:c.2618G>T
|
XP_006724629.1:p.Cys873Phe
|
|
XM_011543993.2:c.2741G>T
|
XP_011542295.1:p.Cys914Phe
|
|
XM_011543994.2:c.2705G>T
|
XP_011542296.1:p.Cys902Phe
|
|
XM_011543995.2:c.2672G>T
|
XP_011542297.1:p.Cys891Phe
|
|
XM_011543996.2:c.2636G>T
|
XP_011542298.1:p.Cys879Phe
|
|
XM_011543997.3:c.2168G>T
|
XP_011542299.1:p.Cys723Phe
|
|
XM_024452473.1:c.2063G>T
|
XP_024308241.1:p.Cys688Phe
|
|
NM_001367721.1:c.2741G>T
MANE Select
|
NP_001354650.1:p.Cys914Phe
|
|