ENST00000327155.10:c.139C>T
MANE Select
|
ENSP00000323050.5:p.Gln47Ter
|
|
ENST00000327155.9:c.139C>T
|
ENSP00000323050.5:p.Gln47Ter
|
|
ENST00000360790.9:c.139C>T
|
ENSP00000354024.5:p.Gln47Ter
|
|
ENST00000399721.6:c.139C>T
|
ENSP00000382627.2:p.Gln47Ter
|
|
ENST00000399722.6:c.139C>T
|
ENSP00000382628.2:p.Gln47Ter
|
|
ENST00000399725.6:c.139C>T
|
ENSP00000382630.2:p.Gln47Ter
|
|
ENST00000579124.5:c.139C>T
|
ENSP00000462390.1:p.Gln47Ter
|
|
ENST00000580892.1:n.135C>T
|
|
|
ENST00000581819.5:c.139C>T
|
ENSP00000463439.1:p.Gln47Ter
|
|
ENST00000582354.5:c.139C>T
|
ENSP00000463738.1:p.Gln47Ter
|
|
NM_002894.2:c.139C>T
|
NP_002885.1:p.Gln47Ter
|
|
NM_203291.1:c.139C>T
|
NP_976036.1:p.Gln47Ter
|
|
NM_203292.1:c.139C>T
|
NP_976037.1:p.Gln47Ter
|
|
XM_005258325.1:c.139C>T
|
XP_005258382.1:p.Gln47Ter
|
|
XM_006722519.1:c.139C>T
|
XP_006722582.1:p.Gln47Ter
|
|
XM_006722520.1:c.139C>T
|
XP_006722583.1:p.Gln47Ter
|
|
XM_006722521.1:c.139C>T
|
XP_006722584.1:p.Gln47Ter
|
|
XM_011526132.1:c.139C>T
|
XP_011524434.1:p.Gln47Ter
|
|
XM_005258325.3:c.139C>T
|
XP_005258382.1:p.Gln47Ter
|
|
XM_005258326.4:c.-778C>T
|
XP_005258383.1:n.-778C>T
|
|
XM_006722519.2:c.139C>T
|
XP_006722582.1:p.Gln47Ter
|
|
XM_006722520.2:c.139C>T
|
XP_006722583.1:p.Gln47Ter
|
|
XM_006722521.2:c.139C>T
|
XP_006722584.1:p.Gln47Ter
|
|
XM_011526132.2:c.139C>T
|
XP_011524434.1:p.Gln47Ter
|
|
XM_017025916.1:c.-844C>T
|
XP_016881405.1:n.-844C>T
|
|
XM_024451233.1:c.-222C>T
|
XP_024307001.1:n.-222C>T
|
|
NM_002894.3:c.139C>T
MANE Select
|
NP_002885.1:p.Gln47Ter
|
|
NM_203291.2:c.139C>T
|
NP_976036.1:p.Gln47Ter
|
|
NM_203292.2:c.139C>T
|
NP_976037.1:p.Gln47Ter
|
|