ENST00000366963.9:c.1498+307G>T
MANE Select
|
ENSP00000355930.4:n.1498+307G>T
|
|
ENST00000324965.8:c.1386-758G>T
|
ENSP00000318103.4:n.1386-758G>T
|
|
ENST00000366963.8:c.1498+307G>T
|
ENSP00000355930.4:n.1498+307G>T
|
|
ENST00000457470.6:c.1386-3299G>T
|
ENSP00000409557.2:n.1386-3299G>T
|
|
ENST00000460902.2:c.1283+307G>T
|
ENSP00000439274.1:n.1283+307G>T
|
|
ENST00000539263.5:c.*971+307G>T
|
ENSP00000443245.1:n.*971+307G>T
|
|
NM_003057.2:c.1498+307G>T
|
NP_003048.1:n.1498+307G>T
|
|
NM_153187.1:c.1386-758G>T
|
NP_694857.1:n.1386-758G>T
|
|
XM_005267102.3:c.1498+307G>T
|
XP_005267159.1:n.1498+307G>T
|
|
XM_005267103.1:c.1499-213G>T
|
XP_005267160.1:n.1499-213G>T
|
|
XM_005267104.3:c.922+307G>T
|
XP_005267161.1:n.922+307G>T
|
|
XM_005267105.3:c.922+307G>T
|
XP_005267162.1:n.922+307G>T
|
|
XM_006715552.1:c.1386-3299G>T
|
XP_006715615.1:n.1386-3299G>T
|
|
XM_011536074.1:c.922+307G>T
|
XP_011534376.1:n.922+307G>T
|
|
XM_005267102.5:c.1498+307G>T
|
XP_005267159.1:n.1498+307G>T
|
|
XM_005267103.2:c.1499-213G>T
|
XP_005267160.1:n.1499-213G>T
|
|
XM_005267104.5:c.922+307G>T
|
XP_005267161.1:n.922+307G>T
|
|
XM_005267105.5:c.922+307G>T
|
XP_005267162.1:n.922+307G>T
|
|
XM_006715552.2:c.1386-3299G>T
|
XP_006715615.1:n.1386-3299G>T
|
|
XM_011536074.3:c.922+307G>T
|
XP_011534376.1:n.922+307G>T
|
|
NM_003057.3:c.1498+307G>T
MANE Select
|
NP_003048.1:n.1498+307G>T
|
|
NM_153187.2:c.1386-758G>T
|
NP_694857.1:n.1386-758G>T
|
|