ENST00000029410.10:c.813C>G
MANE Select
|
ENSP00000029410.5:p.Ile271Met
|
|
ENST00000029410.9:c.813C>G
|
ENSP00000029410.5:p.Ile271Met
|
|
ENST00000505145.1:n.1911C>G
|
|
|
ENST00000505433.5:c.*319C>G
|
ENSP00000425591.1:n.*319C>G
|
|
ENST00000515353.1:n.1635C>G
|
|
|
NM_007255.2:c.813C>G
|
NP_009186.1:p.Ile271Met
|
|
XM_005265805.2:c.471C>G
|
XP_005265862.1:p.Ile157Met
|
|
XM_006714816.2:c.333C>G
|
XP_006714879.1:p.Ile111Met
|
|
XM_011534421.1:c.471C>G
|
XP_011532723.1:p.Ile157Met
|
|
XM_006714816.4:c.333C>G
|
XP_006714879.1:p.Ile111Met
|
|
XM_017008999.2:c.471C>G
|
XP_016864488.1:p.Ile157Met
|
|
NM_007255.3:c.813C>G
MANE Select
|
NP_009186.1:p.Ile271Met
|
|