ENST00000366159.9:n.294G>T
|
|
|
ENST00000437813.8:c.260G>T
|
ENSP00000513672.1:p.Gly87Val
|
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ENST00000440083.7:c.260G>T
|
ENSP00000413224.3:p.Gly87Val
|
|
ENST00000535958.2:c.*87G>T
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ENSP00000513673.1:n.*87G>T
|
|
ENST00000698339.1:c.260G>T
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ENSP00000513670.1:p.Gly87Val
|
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ENST00000698340.1:c.260G>T
|
ENSP00000513671.1:p.Gly87Val
|
|
ENST00000162749.7:c.260G>T
MANE Select
|
ENSP00000162749.2:p.Gly87Val
|
|
ENST00000162749.6:c.260G>T
|
ENSP00000162749.2:p.Gly87Val
|
|
ENST00000366159.8:c.260G>T
|
ENSP00000380389.3:p.Gly87Val
|
|
ENST00000437813.7:n.221G>T
|
|
|
ENST00000440083.6:c.260G>T
|
ENSP00000413224.2:p.Gly87Val
|
|
ENST00000534885.5:c.106G>T
|
ENSP00000441803.1:p.Ala36Ser
|
|
ENST00000535958.1:n.506G>T
|
|
|
ENST00000536194.1:c.233G>T
|
ENSP00000442919.1:p.Gly78Val
|
|
ENST00000539372.5:c.260G>T
|
ENSP00000442059.1:p.Gly87Val
|
|
ENST00000540022.5:c.194-283G>T
|
ENSP00000438343.1:n.194-283G>T
|
|
ENST00000543048.5:c.214+46G>T
|
ENSP00000439981.1:n.214+46G>T
|
|
ENST00000543995.5:c.193+292G>T
|
ENSP00000442405.1:n.193+292G>T
|
|
NM_001065.3:c.260G>T , LRG_193t1:c.260G>T
|
NP_001056.1:p.Gly87Val
|
|
NM_001346091.1:c.-65G>T
|
NP_001333020.1:n.-65G>T
|
|
NM_001346092.1:c.-318G>T
|
NP_001333021.1:n.-318G>T
|
|
NR_144351.1:n.563G>T
|
|
|
NM_001065.4:c.260G>T
MANE Select
|
NP_001056.1:p.Gly87Val
|
|
NM_001346091.2:c.-65G>T
|
NP_001333020.1:n.-65G>T
|
|
NM_001346092.2:c.-318G>T
|
NP_001333021.1:n.-318G>T
|
|
NR_144351.2:n.522G>T
|
|
|