ENST00000252137.11:c.*2464G>A
(ESS2)
MANE Select
|
ENSP00000252137.6:n.*2464G>A
|
|
ENST00000399635.4:c.333C>T
(TSSK2)
MANE Select
|
ENSP00000382544.2:p.Asp111=
|
|
ENST00000252137.10:c.*2464G>A
(ESS2)
|
ENSP00000252137.6:n.*2464G>A
|
|
ENST00000399635.3:c.333C>T
(TSSK2)
|
ENSP00000382544.2:p.Asp111=
|
|
NM_022719.2:c.*2464G>A
(ESS2)
|
NP_073210.1:n.*2464G>A
|
|
NM_053006.4:c.333C>T
(TSSK2)
|
NP_443732.3:p.Asp111=
|
|
XM_005261282.3:c.*2464G>A
(ESS2)
|
XP_005261339.1:n.*2464G>A
|
|
XM_006724329.2:c.*2464G>A
(ESS2)
|
XP_006724392.1:n.*2464G>A
|
|
XM_006724330.2:c.*2464G>A
(ESS2)
|
XP_006724393.1:n.*2464G>A
|
|
XM_006724331.2:c.*2464G>A
(ESS2)
|
XP_006724394.1:n.*2464G>A
|
|
XR_937926.1:n.3853G>A
(ESS2)
|
|
|
NR_134304.1:n.4009G>A
(ESS2)
|
|
|
NM_022719.3:c.*2464G>A
(ESS2)
MANE Select
|
NP_073210.1:n.*2464G>A
|
|
NM_053006.5:c.333C>T
(TSSK2)
MANE Select
|
NP_443732.3:p.Asp111=
|
|
NR_134304.2:n.3983G>A
(ESS2)
|
|
|