ENST00000394867.9:n.1804T>C
|
|
|
ENST00000688751.1:n.501T>C
|
|
|
ENST00000689792.1:n.1269T>C
|
|
|
ENST00000262948.10:c.*162T>C
MANE Select
|
ENSP00000262948.4:n.*162T>C
|
|
ENST00000262948.9:c.*162T>C
|
ENSP00000262948.3:n.*162T>C
|
|
ENST00000394867.8:c.*162T>C
|
ENSP00000378336.1:n.*162T>C
|
|
ENST00000597263.5:n.550T>C
|
|
|
ENST00000600584.5:n.2814T>C
|
|
|
ENST00000601786.5:n.1666T>C
|
|
|
NM_030662.3:c.*162T>C , LRG_750t1:c.*162T>C
|
NP_109587.1:n.*162T>C
|
|
XM_006722799.2:c.*162T>C
|
XP_006722862.1:n.*162T>C
|
|
XM_011528133.1:c.*162T>C
|
XP_011526435.1:n.*162T>C
|
|
NM_030662.4:c.*162T>C
MANE Select
|
NP_109587.1:n.*162T>C
|
|