ENST00000449291.7:c.1217T>G
MANE Select
|
ENSP00000401508.2:p.Met406Arg
|
|
ENST00000340490.7:c.1217T>G
|
ENSP00000341136.3:p.Met406Arg
|
|
ENST00000426292.7:c.1217T>G
|
ENSP00000390949.3:p.Met406Arg
|
|
ENST00000435154.7:c.1217T>G
|
ENSP00000405670.3:p.Met406Arg
|
|
ENST00000449291.6:c.1217T>G
|
ENSP00000401508.2:p.Met406Arg
|
|
ENST00000460623.5:c.195T>G
|
|
|
ENST00000464332.5:n.761T>G
|
|
|
ENST00000525583.5:c.1001T>G
|
|
|
NM_001286829.1:c.1217T>G
|
NP_001273758.1:p.Met406Arg
|
|
NM_145201.5:c.1217T>G
|
NP_660202.3:p.Met406Arg
|
|
XM_011517377.1:c.1217T>G
|
XP_011515679.1:p.Met406Arg
|
|
NM_001363145.1:c.1136T>G
|
NP_001350074.1:p.Met379Arg
|
|
NM_001363146.1:c.533T>G
|
NP_001350075.1:p.Met178Arg
|
|
XM_017013975.2:c.1436T>G
|
XP_016869464.1:p.Met479Arg
|
|
XM_017013976.2:c.1436T>G
|
XP_016869465.1:p.Met479Arg
|
|
XM_017013977.2:c.1136T>G
|
XP_016869466.1:p.Met379Arg
|
|
XM_017013978.2:c.1436T>G
|
XP_016869467.1:p.Met479Arg
|
|
XM_017013979.2:c.533T>G
|
XP_016869468.1:p.Met178Arg
|
|
XM_024447332.1:c.854T>G
|
XP_024303100.1:p.Met285Arg
|
|
XM_024447333.1:c.452T>G
|
XP_024303101.1:p.Met151Arg
|
|
NM_145201.6:c.1217T>G
MANE Select
|
NP_660202.3:p.Met406Arg
|
|
NM_001286829.2:c.1217T>G
|
NP_001273758.1:p.Met406Arg
|
|