ENST00000352909.8:c.949G>C
MANE Select
|
ENSP00000325951.4:p.Ala317Pro
|
|
ENST00000324155.8:c.*638G>C
|
ENSP00000325831.3:n.*638G>C
|
|
ENST00000333684.9:c.696-112G>C
|
ENSP00000328814.6:n.696-112G>C
|
|
ENST00000352909.7:c.949G>C
|
ENSP00000325951.3:p.Ala317Pro
|
|
ENST00000381168.7:c.*669G>C
|
ENSP00000370560.3:n.*669G>C
|
|
ENST00000381175.5:c.1030G>C
|
ENSP00000370567.1:p.Ala344Pro
|
|
ENST00000381178.5:c.1042G>C
|
ENSP00000370571.1:p.Ala348Pro
|
|
ENST00000412076.1:c.136-112G>C
|
|
|
ENST00000416223.5:c.243G>C
|
|
|
ENST00000461172.1:n.114G>C
|
|
|
ENST00000479437.5:n.498G>C
|
|
|
NM_000360.3:c.949G>C
|
NP_000351.2:p.Ala317Pro
|
|
NM_199292.2:c.1042G>C
|
NP_954986.2:p.Ala348Pro
|
|
NM_199293.2:c.1030G>C
|
NP_954987.2:p.Ala344Pro
|
|
XM_011520335.1:c.961G>C
|
XP_011518637.1:p.Ala321Pro
|
|
XM_011520335.2:c.961G>C
|
XP_011518637.1:p.Ala321Pro
|
|
NM_000360.4:c.949G>C
MANE Select
|
NP_000351.2:p.Ala317Pro
|
|
NM_199292.3:c.1042G>C
|
NP_954986.2:p.Ala348Pro
|
|
NM_199293.3:c.1030G>C
|
NP_954987.2:p.Ala344Pro
|
|