ENST00000684779.1:c.628-2107T=
|
ENSP00000508681.1:n.628-2107T=
|
|
ENST00000685172.1:c.825T=
|
ENSP00000509604.1:p.Phe275=
|
|
ENST00000685763.1:c.678T=
|
ENSP00000509016.1:p.Phe226=
|
|
ENST00000686347.1:c.569-2107T=
|
ENSP00000509027.1:n.569-2107T=
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ENST00000687191.1:n.1183T=
|
|
|
ENST00000687481.1:n.240T=
|
|
|
ENST00000689951.1:c.876T=
|
ENSP00000509308.1:p.Phe292=
|
|
ENST00000691077.1:c.*62T=
|
ENSP00000509843.1:n.*62T=
|
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ENST00000691576.1:c.696T=
|
ENSP00000510066.1:p.Phe232=
|
|
ENST00000691937.1:c.825T=
|
ENSP00000508768.1:p.Phe275=
|
|
ENST00000692487.1:c.*62T=
|
ENSP00000509534.1:n.*62T=
|
|
ENST00000692683.1:c.759T=
|
ENSP00000508437.1:p.Phe253=
|
|
ENST00000693150.1:c.681T=
|
ENSP00000510309.1:p.Phe227=
|
|
ENST00000307102.10:c.825T=
MANE Select
|
ENSP00000302486.5:p.Phe275=
|
|
ENST00000307102.9:c.825T=
|
ENSP00000302486.4:p.Phe275=
|
|
ENST00000566326.1:c.297T=
|
ENSP00000456438.1:p.Phe99=
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|
NM_002755.3:c.825T= , LRG_725t1:c.825T=
|
NP_002746.1:p.Phe275=
|
|
XM_011521783.1:c.759T=
|
XP_011520085.1:p.Phe253=
|
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XM_011521783.3:c.759T=
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XP_011520085.1:p.Phe253=
|
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XM_017022411.2:c.747T=
|
XP_016877900.1:p.Phe249=
|
|
XM_017022412.1:c.681T=
|
XP_016877901.1:p.Phe227=
|
|
XM_017022413.1:c.297T=
|
XP_016877902.1:p.Phe99=
|
|
NM_002755.4:c.825T=
MANE Select
|
NP_002746.1:p.Phe275=
|
|