ENST00000324071.10:c.1281C>G
MANE Select
|
ENSP00000324648.2:p.Ile427Met
|
|
ENST00000598834.2:c.1177-171C>G
|
|
|
ENST00000324071.8:c.1281C>G
|
ENSP00000324648.2:p.Ile427Met
|
|
ENST00000593831.1:c.573C>G
|
ENSP00000470582.1:p.Ile191Met
|
|
ENST00000597612.1:n.647+317C>G
|
|
|
NM_000767.4:c.1281C>G
|
NP_000758.1:p.Ile427Met
|
|
XM_005258569.3:c.1152+317C>G
|
XP_005258626.1:n.1152+317C>G
|
|
XM_006723050.2:c.1281C>G
|
XP_006723113.1:p.Ile427Met
|
|
XM_011526546.1:c.1153-14C>G
|
XP_011524848.1:n.1153-14C>G
|
|
XM_011526547.1:c.1153-171C>G
|
XP_011524849.1:n.1153-171C>G
|
|
XM_011526548.1:c.801C>G
|
XP_011524850.1:p.Ile267Met
|
|
XM_011526549.1:c.690C>G
|
XP_011524851.1:p.Ile230Met
|
|
XM_011526550.1:c.681C>G
|
XP_011524852.1:p.Ile227Met
|
|
NM_000767.5:c.1281C>G
MANE Select
|
NP_000758.1:p.Ile427Met
|
|