|
ENST00000508896.7:c.5185A>T
|
ENSP00000423372.3:p.Asn1729Tyr
|
|
|
ENST00000347982.9:c.5185A>T
|
ENSP00000343209.5:p.Asn1729Tyr
|
|
|
ENST00000354179.9:c.5185A>T
|
ENSP00000346111.5:p.Asn1729Tyr
|
|
|
ENST00000503056.6:c.700A>T
|
ENSP00000424024.2:p.Asn234Tyr
|
|
|
ENST00000508029.6:c.700A>T
|
ENSP00000425120.2:p.Asn234Tyr
|
|
|
ENST00000685206.1:n.5641A>T
|
|
|
|
ENST00000686993.1:c.5185A>T
|
ENSP00000510020.1:p.Asn1729Tyr
|
|
|
ENST00000687453.1:c.5749A>T
|
ENSP00000508426.1:p.Asn1917Tyr
|
|
|
ENST00000688613.1:n.5455A>T
|
|
|
|
ENST00000689345.1:c.5185A>T
|
ENSP00000509711.1:p.Asn1729Tyr
|
|
|
ENST00000689549.1:n.6205A>T
|
|
|
|
ENST00000692024.1:n.4607A>T
|
|
|
|
ENST00000439151.7:c.6058A>T
MANE Select
|
ENSP00000395929.2:p.Asn2020Tyr
|
|
|
ENST00000347982.8:c.5251A>T
|
ENSP00000343209.4:p.Asn1751Tyr
|
|
|
ENST00000354179.8:c.5251A>T
|
ENSP00000346111.4:p.Asn1751Tyr
|
|
|
ENST00000439151.6:c.6058A>T
|
ENSP00000395929.2:p.Asn2020Tyr
|
|
|
NM_022455.4:c.6058A>T , LRG_512t1:c.6058A>T
|
NP_071900.2:p.Asn2020Tyr
|
|
|
NM_172349.2:c.5251A>T
|
NP_758859.1:p.Asn1751Tyr
|
|
|
XM_005265959.1:c.6058A>T
|
XP_005266016.1:p.Asn2020Tyr
|
|
|
XM_005265960.1:c.5251A>T
|
XP_005266017.1:p.Asn1751Tyr
|
|
|
XM_005265961.1:c.5251A>T
|
XP_005266018.1:p.Asn1751Tyr
|
|
|
XM_005265962.3:c.1552A>T
|
XP_005266019.1:p.Asn518Tyr
|
|
|
XM_011534610.1:c.6058A>T
|
XP_011532912.1:p.Asn2020Tyr
|
|
|
XM_011534611.1:c.6058A>T
|
XP_011532913.1:p.Asn2020Tyr
|
|
|
XM_011534612.1:c.5638A>T
|
XP_011532914.1:p.Asn1880Tyr
|
|
|
XM_011534613.1:c.5002A>T
|
XP_011532915.1:p.Asn1668Tyr
|
|
|
XM_011534617.1:c.1792A>T
|
XP_011532919.1:p.Asn598Tyr
|
|
|
NM_001365684.1:c.5251A>T
|
NP_001352613.1:p.Asn1751Tyr
|
|
|
XM_024446150.1:c.6058A>T
|
XP_024301918.1:p.Asn2020Tyr
|
|
|
XM_024446151.1:c.6058A>T
|
XP_024301919.1:p.Asn2020Tyr
|
|
|
XM_024446152.1:c.6058A>T
|
XP_024301920.1:p.Asn2020Tyr
|
|
|
XM_024446153.1:c.6058A>T
|
XP_024301921.1:p.Asn2020Tyr
|
|
|
XM_024446154.1:c.5638A>T
|
XP_024301922.1:p.Asn1880Tyr
|
|
|
XM_024446155.1:c.5251A>T
|
XP_024301923.1:p.Asn1751Tyr
|
|
|
XM_024446156.1:c.5251A>T
|
XP_024301924.1:p.Asn1751Tyr
|
|
|
XM_024446158.1:c.5251A>T
|
XP_024301926.1:p.Asn1751Tyr
|
|
|
XM_024446159.1:c.5002A>T
|
XP_024301927.1:p.Asn1668Tyr
|
|
|
XM_024446162.1:c.1792A>T
|
XP_024301930.1:p.Asn598Tyr
|
|
|
XM_024446163.1:c.1552A>T
|
XP_024301931.1:p.Asn518Tyr
|
|
|
NM_022455.5:c.6058A>T
MANE Select
|
NP_071900.2:p.Asn2020Tyr
|
|
|
NM_172349.3:c.5251A>T
|
NP_758859.1:p.Asn1751Tyr
|
|
