|
NM_005060.4:c.1427G>C
MANE Select
|
NP_005051.2:p.Cys476Ser
|
|
ENST00000318247.7:c.1427G>C
MANE Select
|
ENSP00000327025.6:p.Cys476Ser
|
|
NM_001001523.1:c.1364G>C
|
NP_001001523.1:p.Cys455Ser
|
|
NM_001001523.2:c.1364G>C
|
NP_001001523.1:p.Cys455Ser
|
|
NM_005060.3:c.1427G>C
|
NP_005051.2:p.Cys476Ser
|
|
ENST00000318247.6:c.1427G>C
|
ENSP00000327025.6:p.Cys476Ser
|
|
ENST00000356728.10:c.1364G>C
|
ENSP00000349164.6:p.Cys455Ser
|
|
ENST00000356728.11:c.1364G>C
|
ENSP00000349164.6:p.Cys455Ser
|
|
ENST00000480719.1:n.3497G>C
|
|
|
ENST00000638901.1:c.1618G>C
|
|
|
ENST00000651814.1:c.*384G>C
|
ENSP00000498691.1:n.*384G>C
|
|
ENST00000651893.1:c.704G>C
|
|
|
ENST00000652040.2:c.1142G>C
|
ENSP00000498548.2:p.Cys381Ser
|
|
ENST00000697811.1:c.*109G>C
|
ENSP00000513447.1:n.*109G>C
|
|
XM_006711484.2:c.1826G>C
|
XP_006711547.2:p.Cys609Ser
|
|
XM_006711484.4:c.1826G>C
|
XP_006711547.2:p.Cys609Ser
|
|
XR_426792.2:n.2188G>C
|
|