|
ENST00000445061.6:c.2381T>G
MANE Select
|
ENSP00000405620.1:p.Leu794Trp
|
|
|
ENST00000348968.8:c.2297T>G
|
ENSP00000343442.4:p.Leu766Trp
|
|
|
ENST00000395745.6:c.*2281T>G
|
ENSP00000379094.2:n.*2281T>G
|
|
|
ENST00000445061.5:c.2381T>G
|
ENSP00000405620.1:p.Leu794Trp
|
|
|
ENST00000446256.6:c.2381T>G
|
ENSP00000392601.3:p.Leu794Trp
|
|
|
ENST00000457607.1:c.2465T>G
|
ENSP00000394682.1:p.Leu822Trp
|
|
|
ENST00000474183.1:n.498T>G
|
|
|
|
ENST00000619982.4:c.2264T>G
|
ENSP00000483160.1:p.Leu755Trp
|
|
|
NM_014966.3:c.2264T>G
|
NP_055781.2:p.Leu755Trp
|
|
|
NM_138615.2:c.2381T>G
|
NP_619520.1:p.Leu794Trp
|
|
|
XM_006713033.1:c.2285T>G
|
XP_006713096.1:p.Leu762Trp
|
|
|
XM_011533490.1:c.2594T>G
|
XP_011531792.1:p.Leu865Trp
|
|
|
XM_011533491.1:c.2594T>G
|
XP_011531793.1:p.Leu865Trp
|
|
|
XM_011533492.1:c.2594T>G
|
XP_011531794.1:p.Leu865Trp
|
|
|
XM_011533493.1:c.2483T>G
|
XP_011531795.1:p.Leu828Trp
|
|
|
XM_011533494.1:c.2381T>G
|
XP_011531796.1:p.Leu794Trp
|
|
|
XM_011533495.1:c.2381T>G
|
XP_011531797.1:p.Leu794Trp
|
|
|
XM_011533496.1:c.2297T>G
|
XP_011531798.1:p.Leu766Trp
|
|
|
XM_011533497.1:c.2297T>G
|
XP_011531799.1:p.Leu766Trp
|
|
|
XM_011533498.1:c.2297T>G
|
XP_011531800.1:p.Leu766Trp
|
|
|
NM_001330990.1:c.2297T>G
|
NP_001317919.1:p.Leu766Trp
|
|
|
XM_011533490.2:c.2594T>G
|
XP_011531792.1:p.Leu865Trp
|
|
|
XM_011533494.3:c.2381T>G
|
XP_011531796.1:p.Leu794Trp
|
|
|
XM_011533495.2:c.2381T>G
|
XP_011531797.1:p.Leu794Trp
|
|
|
XM_011533497.2:c.2297T>G
|
XP_011531799.1:p.Leu766Trp
|
|
|
XM_017005914.1:c.2513T>G
|
XP_016861403.1:p.Leu838Trp
|
|
|
XM_017005915.1:c.2285T>G
|
XP_016861404.1:p.Leu762Trp
|
|
|
XM_017005916.2:c.2270T>G
|
XP_016861405.1:p.Leu757Trp
|
|
|
XM_017005917.1:c.2264T>G
|
XP_016861406.1:p.Leu755Trp
|
|
|
XM_024453405.1:c.2483T>G
|
XP_024309173.1:p.Leu828Trp
|
|
|
NM_138615.3:c.2381T>G
MANE Select
|
NP_619520.1:p.Leu794Trp
|
|
|
NM_001330990.2:c.2297T>G
|
NP_001317919.1:p.Leu766Trp
|
|
|
NM_014966.4:c.2264T>G
|
NP_055781.2:p.Leu755Trp
|
|
