ENST00000695850.1:n.1640G>A
|
|
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ENST00000695852.1:n.571G>A
|
|
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ENST00000695853.1:c.*1523G>A
|
ENSP00000512218.1:n.*1523G>A
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|
ENST00000423902.7:c.8464G>A
MANE Select
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ENSP00000392028.1:p.Ala2822Thr
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|
ENST00000423902.6:c.8464G>A
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ENSP00000392028.1:p.Ala2822Thr
|
|
ENST00000524602.5:c.2317G>A
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ENSP00000437061.1:p.Ala773Thr
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|
ENST00000528280.1:n.510G>A
|
|
|
NM_001316690.1:c.2317G>A
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NP_001303619.1:p.Ala773Thr
|
|
NM_017780.3:c.8464G>A
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NP_060250.2:p.Ala2822Thr
|
|
XM_011517553.1:c.8554G>A
|
XP_011515855.1:p.Ala2852Thr
|
|
XM_011517554.1:c.8554G>A
|
XP_011515856.1:p.Ala2852Thr
|
|
XM_011517555.1:c.8551G>A
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XP_011515857.1:p.Ala2851Thr
|
|
XM_011517556.1:c.8332G>A
|
XP_011515858.1:p.Ala2778Thr
|
|
XM_011517557.1:c.6541G>A
|
XP_011515859.1:p.Ala2181Thr
|
|
XM_011517558.1:c.6091G>A
|
XP_011515860.1:p.Ala2031Thr
|
|
XM_011517559.1:c.5299G>A
|
XP_011515861.1:p.Ala1767Thr
|
|
XM_011517553.2:c.8554G>A
|
XP_011515855.1:p.Ala2852Thr
|
|
XM_011517554.3:c.8554G>A
|
XP_011515856.1:p.Ala2852Thr
|
|
XM_011517555.2:c.8551G>A
|
XP_011515857.1:p.Ala2851Thr
|
|
XM_017013612.1:c.8554G>A
|
XP_016869101.1:p.Ala2852Thr
|
|
XM_017013613.1:c.8461G>A
|
XP_016869102.1:p.Ala2821Thr
|
|
NM_017780.4:c.8464G>A
MANE Select
|
NP_060250.2:p.Ala2822Thr
|
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