ENST00000225171.7:c.297+16G>T
MANE Select
|
ENSP00000225171.2:n.297+16G>T
|
|
ENST00000225171.6:c.297+16G>T
|
ENSP00000225171.2:n.297+16G>T
|
|
ENST00000339758.7:c.313G>T
|
ENSP00000343575.6:p.Gly105Cys
|
|
ENST00000480963.5:c.*217+16G>T
|
ENSP00000473979.1:n.*217+16G>T
|
|
ENST00000483798.6:c.387+16G>T
|
ENSP00000474215.1:n.387+16G>T
|
|
NM_021800.2:c.297+16G>T
|
NP_068572.1:n.297+16G>T
|
|
NM_201262.1:c.313G>T
|
NP_957714.1:p.Gly105Cys
|
|
XM_011539967.1:c.327+16G>T
|
XP_011538269.1:n.327+16G>T
|
|
XM_017016431.1:c.51+16G>T
|
XP_016871920.1:n.51+16G>T
|
|
XM_017016432.2:c.51+16G>T
|
XP_016871921.1:n.51+16G>T
|
|
NM_021800.3:c.297+16G>T
MANE Select
|
NP_068572.1:n.297+16G>T
|
|
NM_201262.2:c.313G>T
|
NP_957714.1:p.Gly105Cys
|
|