ENST00000324071.10:c.1093A>G
MANE Select
|
ENSP00000324648.2:p.Met365Val
|
|
ENST00000598834.2:c.1117A>G
|
|
|
ENST00000324071.8:c.1093A>G
|
ENSP00000324648.2:p.Met365Val
|
|
ENST00000593831.1:c.385A>G
|
ENSP00000470582.1:p.Met129Val
|
|
ENST00000597612.1:n.588A>G
|
|
|
NM_000767.4:c.1093A>G
|
NP_000758.1:p.Met365Val
|
|
XM_005258569.3:c.1093A>G
|
XP_005258626.1:p.Met365Val
|
|
XM_006723050.2:c.1093A>G
|
XP_006723113.1:p.Met365Val
|
|
XM_011526546.1:c.1093A>G
|
XP_011524848.1:p.Met365Val
|
|
XM_011526547.1:c.1093A>G
|
XP_011524849.1:p.Met365Val
|
|
XM_011526548.1:c.613A>G
|
XP_011524850.1:p.Met205Val
|
|
XM_011526549.1:c.502A>G
|
XP_011524851.1:p.Met168Val
|
|
XM_011526550.1:c.493A>G
|
XP_011524852.1:p.Met165Val
|
|
NM_000767.5:c.1093A>G
MANE Select
|
NP_000758.1:p.Met365Val
|
|