ENST00000294304.12:c.4489A>G
MANE Select
|
ENSP00000294304.6:p.Ile1497Val
|
|
ENST00000294304.11:c.4489A>G
|
ENSP00000294304.6:p.Ile1497Val
|
|
ENST00000529702.1:c.159A>G
|
|
|
ENST00000529993.5:c.*3095A>G
|
ENSP00000436652.1:n.*3095A>G
|
|
NM_001291902.1:c.2746A>G
|
NP_001278831.1:p.Ile916Val
|
|
NM_002335.3:c.4489A>G
|
NP_002326.2:p.Ile1497Val
|
|
XM_005273994.2:c.4603A>G
|
XP_005274051.1:p.Ile1535Val
|
|
XM_011545029.1:c.4630A>G
|
XP_011543331.1:p.Ile1544Val
|
|
XM_011545030.1:c.4516A>G
|
XP_011543332.1:p.Ile1506Val
|
|
XM_011545031.1:c.4646A>G
|
XP_011543333.1:p.Asp1549Gly
|
|
XR_949925.1:n.4645A>G
|
|
|
XR_949926.1:n.4661A>G
|
|
|
XM_017017735.1:c.2860A>G
|
XP_016873224.1:p.Ile954Val
|
|
XM_017017736.1:c.2143A>G
|
XP_016873225.1:p.Ile715Val
|
|
XR_949925.2:n.4645A>G
|
|
|
XR_949926.2:n.4661A>G
|
|
|
NM_002335.4:c.4489A>G
MANE Select
|
NP_002326.2:p.Ile1497Val
|
|
NM_001291902.2:c.2746A>G
|
NP_001278831.1:p.Ile916Val
|
|