ENST00000368985.8:c.961G>T
MANE Select
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ENSP00000357981.3:p.Gly321Trp
|
|
ENST00000448301.7:c.733G>T
|
ENSP00000408414.2:p.Gly245Trp
|
|
ENST00000472977.7:c.961G>T
|
ENSP00000475176.2:p.Gly321Trp
|
|
ENST00000483930.2:c.*155G>T
|
ENSP00000475812.2:n.*155G>T
|
|
ENST00000607427.2:c.961G>T
|
ENSP00000475557.2:p.Gly321Trp
|
|
ENST00000679512.1:c.858G>T
|
ENSP00000505113.1:p.Val286=
|
|
ENST00000679898.1:c.688G>T
|
ENSP00000505326.1:p.Gly230Trp
|
|
ENST00000680288.1:c.811G>T
|
ENSP00000506001.1:p.Gly271Trp
|
|
ENST00000680311.1:c.*44G>T
|
ENSP00000505020.1:n.*44G>T
|
|
ENST00000680471.1:c.*132G>T
|
ENSP00000506603.1:n.*132G>T
|
|
ENST00000680664.1:c.784G>T
|
ENSP00000506248.1:p.Gly262Trp
|
|
ENST00000680931.1:c.*311G>T
|
ENSP00000504934.1:n.*311G>T
|
|
ENST00000681357.1:n.351G>T
|
|
|
ENST00000681444.1:c.961G>T
|
ENSP00000505359.1:p.Gly321Trp
|
|
ENST00000368985.7:c.961G>T
|
ENSP00000357981.3:p.Gly321Trp
|
|
ENST00000448301.6:c.811G>T
|
ENSP00000408414.1:p.Gly271Trp
|
|
ENST00000472977.6:c.254G>T
|
|
|
ENST00000483930.1:c.509G>T
|
ENSP00000475812.1:n.509G>T
|
|
NM_001199739.1:c.811G>T
|
NP_001186668.1:p.Gly271Trp
|
|
NM_004079.4:c.961G>T
|
NP_004070.3:p.Gly321Trp
|
|
NM_004079.5:c.961G>T
MANE Select
|
NP_004070.3:p.Gly321Trp
|
|
NM_001199739.2:c.811G>T
|
NP_001186668.1:p.Gly271Trp
|
|