ENST00000252137.11:c.*1836G>T
(ESS2)
MANE Select
|
ENSP00000252137.6:n.*1836G>T
|
|
ENST00000399635.4:c.961C>A
(TSSK2)
MANE Select
|
ENSP00000382544.2:p.His321Asn
|
|
ENST00000252137.10:c.*1836G>T
(ESS2)
|
ENSP00000252137.6:n.*1836G>T
|
|
ENST00000399635.3:c.961C>A
(TSSK2)
|
ENSP00000382544.2:p.His321Asn
|
|
NM_022719.2:c.*1836G>T
(ESS2)
|
NP_073210.1:n.*1836G>T
|
|
NM_053006.4:c.961C>A
(TSSK2)
|
NP_443732.3:p.His321Asn
|
|
XM_005261282.3:c.*1836G>T
(ESS2)
|
XP_005261339.1:n.*1836G>T
|
|
XM_006724329.2:c.*1836G>T
(ESS2)
|
XP_006724392.1:n.*1836G>T
|
|
XM_006724330.2:c.*1836G>T
(ESS2)
|
XP_006724393.1:n.*1836G>T
|
|
XM_006724331.2:c.*1836G>T
(ESS2)
|
XP_006724394.1:n.*1836G>T
|
|
XR_937926.1:n.3225G>T
(ESS2)
|
|
|
NR_134304.1:n.3381G>T
(ESS2)
|
|
|
NM_022719.3:c.*1836G>T
(ESS2)
MANE Select
|
NP_073210.1:n.*1836G>T
|
|
NM_053006.5:c.961C>A
(TSSK2)
MANE Select
|
NP_443732.3:p.His321Asn
|
|
NR_134304.2:n.3355G>T
(ESS2)
|
|
|