ENST00000584880.6:c.*370G=
|
ENSP00000464347.2:n.*370G=
|
|
ENST00000703608.1:c.*690G=
|
ENSP00000515392.1:n.*690G=
|
|
ENST00000703609.1:c.1092G=
|
ENSP00000515393.1:p.Met364=
|
|
ENST00000703610.1:c.*450G=
|
ENSP00000515394.1:n.*450G=
|
|
ENST00000310144.11:c.1173G=
MANE Select
|
ENSP00000310572.6:p.Met391=
|
|
ENST00000310144.10:c.1173G=
|
ENSP00000310572.6:p.Met391=
|
|
ENST00000375812.8:c.1149G=
|
ENSP00000364970.4:p.Met383=
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ENST00000578570.5:n.1583G=
|
|
|
ENST00000579147.5:n.2488G=
|
|
|
ENST00000580864.5:c.1149G=
|
ENSP00000462495.1:p.Met383=
|
|
ENST00000581882.5:c.1149G=
|
ENSP00000463938.1:p.Met383=
|
|
ENST00000584657.1:n.478G=
|
|
|
ENST00000585242.5:c.*944G=
|
ENSP00000463107.1:n.*944G=
|
|
NM_001199163.1:c.1149G=
|
NP_001186092.1:p.Met383=
|
|
NM_002805.5:c.1173G=
|
NP_002796.4:p.Met391=
|
|
XM_006721980.1:c.1173G=
|
XP_006722043.1:p.Met391=
|
|
XR_934508.1:n.1262G=
|
|
|
XM_024450840.1:c.1254G=
|
XP_024306608.1:p.Met418=
|
|
XM_024450841.1:c.1230G=
|
XP_024306609.1:p.Met410=
|
|
XR_934508.2:n.1249G=
|
|
|
NM_002805.6:c.1173G=
MANE Select
|
NP_002796.4:p.Met391=
|
|
NM_001199163.2:c.1149G=
|
NP_001186092.1:p.Met383=
|
|