ENST00000684910.1:c.*149T>C
|
ENSP00000509844.1:n.*149T>C
|
|
ENST00000685439.1:c.271T>C
|
ENSP00000508454.1:p.Tyr91His
|
|
ENST00000685944.1:c.616T>C
|
ENSP00000509266.1:p.Tyr206His
|
|
ENST00000686212.1:n.218T>C
|
|
|
ENST00000687215.1:c.*371T>C
|
ENSP00000509706.1:n.*371T>C
|
|
ENST00000688152.1:c.*60T>C
|
ENSP00000509360.1:n.*60T>C
|
|
ENST00000688403.1:c.-129T>C
|
ENSP00000508944.1:n.-129T>C
|
|
ENST00000689314.1:c.661T>C
|
ENSP00000510607.1:p.Tyr221His
|
|
ENST00000689694.1:c.616T>C
|
ENSP00000508718.1:p.Tyr206His
|
|
ENST00000689810.1:c.*265T>C
|
ENSP00000510635.1:n.*265T>C
|
|
ENST00000690282.1:c.-129T>C
|
ENSP00000509809.1:n.-129T>C
|
|
ENST00000690351.1:c.*268T>C
|
ENSP00000509728.1:n.*268T>C
|
|
ENST00000691232.1:c.271T>C
|
ENSP00000509675.1:p.Tyr91His
|
|
ENST00000691482.1:n.1631T>C
|
|
|
ENST00000691686.1:c.616T>C
|
ENSP00000509784.1:p.Tyr206His
|
|
ENST00000691851.1:c.616T>C
|
ENSP00000510106.1:p.Tyr206His
|
|
ENST00000692015.1:c.403T>C
|
ENSP00000510634.1:p.Tyr135His
|
|
ENST00000692638.1:c.*421T>C
|
ENSP00000509412.1:n.*421T>C
|
|
ENST00000692852.1:c.616T>C
|
ENSP00000510337.1:p.Tyr206His
|
|
ENST00000692915.1:c.*823T>C
|
ENSP00000508547.1:n.*823T>C
|
|
ENST00000370396.7:c.616T>C
MANE Select
|
ENSP00000359423.3:p.Tyr206His
|
|
ENST00000306167.11:n.483T>C
|
|
|
ENST00000370396.6:c.616T>C
|
ENSP00000359423.2:p.Tyr206His
|
|
ENST00000490530.1:n.555T>C
|
|
|
NM_000252.2:c.616T>C , LRG_839t1:c.616T>C
|
NP_000243.1:p.Tyr206His
|
|
XM_005274687.2:c.616T>C
|
XP_005274744.1:p.Tyr206His
|
|
XM_011531170.1:c.682T>C
|
XP_011529472.1:p.Tyr228His
|
|
XM_011531171.1:c.661T>C
|
XP_011529473.1:p.Tyr221His
|
|
XM_011531172.1:c.661T>C
|
XP_011529474.1:p.Tyr221His
|
|
XM_011531173.1:c.616T>C
|
XP_011529475.1:p.Tyr206His
|
|
XM_011531173.2:c.616T>C
|
XP_011529475.1:p.Tyr206His
|
|
XM_017029547.1:c.661T>C
|
XP_016885036.1:p.Tyr221His
|
|
XM_017029548.1:c.661T>C
|
XP_016885037.1:p.Tyr221His
|
|
XM_017029549.1:c.616T>C
|
XP_016885038.1:p.Tyr206His
|
|
XM_017029550.1:c.505T>C
|
XP_016885039.1:p.Tyr169His
|
|
XM_017029551.2:c.-129T>C
|
XP_016885040.1:n.-129T>C
|
|
NM_000252.3:c.616T>C
MANE Select
|
NP_000243.1:p.Tyr206His
|
|
NM_001376906.1:c.616T>C
|
NP_001363835.1:p.Tyr206His
|
|
NM_001376907.1:c.505T>C
|
NP_001363836.1:p.Tyr169His
|
|
NM_001376908.1:c.616T>C
|
NP_001363837.1:p.Tyr206His
|
|