ENST00000673913.2:c.*120G>A
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ENSP00000501161.2:n.*120G>A
|
|
ENST00000710286.1:c.2137G>A
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ENSP00000518176.1:p.Ala713Thr
|
|
ENST00000673903.1:c.1405G>A
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ENSP00000501257.1:p.Ala469Thr
|
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ENST00000673913.1:c.630G>A
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ENSP00000501161.1:n.630G>A
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ENST00000302118.5:c.1780G>A
MANE Select
|
ENSP00000303208.5:p.Ala594Thr
|
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ENST00000490692.1:n.2326G>A
|
|
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NM_174936.3:c.1780G>A , LRG_275t1:c.1780G>A
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NP_777596.2:p.Ala594Thr
|
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NR_110451.1:n.1387G>A
|
|
|
XM_011541193.1:c.901G>A
|
XP_011539495.1:p.Ala301Thr
|
|
NM_174936.4:c.1780G>A
MANE Select
|
NP_777596.2:p.Ala594Thr
|
|
NR_110451.2:n.1387G>A
|
|
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