ENST00000315491.12:c.1217T>G
MANE Select
|
ENSP00000320295.7:p.Met406Arg
|
|
ENST00000680788.1:n.4638T>G
|
|
|
ENST00000315491.11:c.1217T>G
|
ENSP00000320295.7:p.Met406Arg
|
|
ENST00000554444.5:c.1001T>G
|
ENSP00000451617.1:p.Met334Arg
|
|
ENST00000555576.5:c.277+2090T>G
|
ENSP00000452554.1:n.277+2090T>G
|
|
ENST00000555609.5:c.*1302T>G
|
ENSP00000451276.1:n.*1302T>G
|
|
ENST00000556922.1:c.2258T>G
|
ENSP00000451560.1:p.Met753Arg
|
|
NM_001197181.1:c.1001T>G
|
NP_001184110.1:p.Met334Arg
|
|
NM_006086.3:c.1217T>G
|
NP_006077.2:p.Met406Arg
|
|
NM_006086.4:c.1217T>G
MANE Select
|
NP_006077.2:p.Met406Arg
|
|
NM_001197181.2:c.1001T>G
|
NP_001184110.1:p.Met334Arg
|
|