ENST00000673913.2:c.1594G>T
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ENSP00000501161.2:p.Ala532Ser
|
|
ENST00000710286.1:c.1951G>T
|
ENSP00000518176.1:p.Ala651Ser
|
|
ENST00000673903.1:c.1219G>T
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ENSP00000501257.1:p.Ala407Ser
|
|
ENST00000673913.1:c.334G>T
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ENSP00000501161.1:p.Ala112Ser
|
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ENST00000302118.5:c.1594G>T
MANE Select
|
ENSP00000303208.5:p.Ala532Ser
|
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ENST00000490692.1:n.2227+929G>T
|
|
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NM_174936.3:c.1594G>T , LRG_275t1:c.1594G>T
|
NP_777596.2:p.Ala532Ser
|
|
NR_110451.1:n.1201G>T
|
|
|
XM_011541193.1:c.715G>T
|
XP_011539495.1:p.Ala239Ser
|
|
NM_174936.4:c.1594G>T
MANE Select
|
NP_777596.2:p.Ala532Ser
|
|
NR_110451.2:n.1201G>T
|
|
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