ENST00000282516.13:c.6942T>C
MANE Select
|
ENSP00000282516.8:p.Ile2314=
|
|
ENST00000652901.1:c.6942T>C
|
ENSP00000499536.1:p.Ile2314=
|
|
ENST00000282516.12:c.6942T>C
|
ENSP00000282516.8:p.Ile2314=
|
|
ENST00000448238.2:c.6942T>C
|
ENSP00000406266.2:p.Ile2314=
|
|
ENST00000621733.1:c.1-15289T>C
|
ENSP00000480694.1:n.1-15289T>C
|
|
NM_015384.4:c.6942T>C
|
NP_056199.2:p.Ile2314=
|
|
NM_133433.3:c.6942T>C
|
NP_597677.2:p.Ile2314=
|
|
XM_005248280.2:c.6942T>C
|
XP_005248337.1:p.Ile2314=
|
|
XM_005248282.3:c.6198T>C
|
XP_005248339.2:p.Ile2066=
|
|
XM_006714467.2:c.6942T>C
|
XP_006714530.1:p.Ile2314=
|
|
XM_006714468.1:c.6744T>C
|
XP_006714531.1:p.Ile2248=
|
|
XM_011514014.1:c.6561T>C
|
XP_011512316.1:p.Ile2187=
|
|
XM_011514015.1:c.6942T>C
|
XP_011512317.1:p.Ile2314=
|
|
XM_005248280.3:c.6942T>C
|
XP_005248337.1:p.Ile2314=
|
|
XM_005248282.5:c.6282T>C
|
XP_005248339.3:p.Ile2094=
|
|
XM_006714468.2:c.6744T>C
|
XP_006714531.1:p.Ile2248=
|
|
XM_017009329.1:c.6942T>C
|
XP_016864818.1:p.Ile2314=
|
|
XM_017009330.2:c.5325T>C
|
XP_016864819.1:p.Ile1775=
|
|
XM_017009331.1:c.5316T>C
|
XP_016864820.1:p.Ile1772=
|
|
NM_133433.4:c.6942T>C
MANE Select
|
NP_597677.2:p.Ile2314=
|
|
NM_015384.5:c.6942T>C
|
NP_056199.2:p.Ile2314=
|
|