ENST00000298139.7:c.3193G>A
MANE Select
|
ENSP00000298139.5:p.Ala1065Thr
|
|
ENST00000650667.1:c.*2807G>A
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ENSP00000498593.1:n.*2807G>A
|
|
ENST00000298139.5:c.3193G>A
|
ENSP00000298139.5:p.Ala1065Thr
|
|
ENST00000521620.5:n.1826G>A
|
|
|
NM_000553.4:c.3193G>A , LRG_524t1:c.3193G>A
|
NP_000544.2:p.Ala1065Thr
|
|
XM_011544639.1:c.3112G>A
|
XP_011542941.1:p.Ala1038Thr
|
|
XM_011544640.1:c.1594G>A
|
XP_011542942.1:p.Ala532Thr
|
|
XR_949470.1:n.3466G>A
|
|
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XR_949471.1:n.3466G>A
|
|
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XR_949472.1:n.3466G>A
|
|
|
NM_000553.5:c.3193G>A
|
NP_000544.2:p.Ala1065Thr
|
|
XM_011544639.3:c.3112G>A
|
XP_011542941.1:p.Ala1038Thr
|
|
XM_024447265.1:c.2983G>A
|
XP_024303033.1:p.Ala995Thr
|
|
XR_949470.3:n.3494G>A
|
|
|
XR_949471.3:n.3494G>A
|
|
|
XR_949472.3:n.3494G>A
|
|
|
NM_000553.6:c.3193G>A
MANE Select
|
NP_000544.2:p.Ala1065Thr
|
|