ENST00000225171.7:c.297+71G>T
MANE Select
|
ENSP00000225171.2:n.297+71G>T
|
|
ENST00000225171.6:c.297+71G>T
|
ENSP00000225171.2:n.297+71G>T
|
|
ENST00000339758.7:c.*44G>T
|
ENSP00000343575.6:n.*44G>T
|
|
ENST00000480963.5:c.*217+71G>T
|
ENSP00000473979.1:n.*217+71G>T
|
|
ENST00000483798.6:c.387+71G>T
|
ENSP00000474215.1:n.387+71G>T
|
|
NM_021800.2:c.297+71G>T
|
NP_068572.1:n.297+71G>T
|
|
NM_201262.1:c.*44G>T
|
NP_957714.1:n.*44G>T
|
|
XM_011539967.1:c.327+71G>T
|
XP_011538269.1:n.327+71G>T
|
|
XM_017016431.1:c.51+71G>T
|
XP_016871920.1:n.51+71G>T
|
|
XM_017016432.2:c.51+71G>T
|
XP_016871921.1:n.51+71G>T
|
|
NM_021800.3:c.297+71G>T
MANE Select
|
NP_068572.1:n.297+71G>T
|
|
NM_201262.2:c.*44G>T
|
NP_957714.1:n.*44G>T
|
|