ENST00000706989.1:c.2432T>G
|
ENSP00000516702.1:p.Val811Gly
|
|
ENST00000359125.7:c.2378T>G
MANE Select
|
ENSP00000352035.2:p.Val793Gly
|
|
ENST00000637193.1:c.1775T>G
|
ENSP00000490734.1:p.Val592Gly
|
|
ENST00000344462.8:c.2285T>G
|
ENSP00000339611.4:p.Val762Gly
|
|
ENST00000357249.6:c.1946T>G
|
ENSP00000349789.3:p.Val649Gly
|
|
ENST00000359125.6:c.2378T>G
|
ENSP00000352035.2:p.Val793Gly
|
|
ENST00000360480.7:c.2294T>G
|
ENSP00000353668.3:p.Val765Gly
|
|
ENST00000370224.5:c.2241+161T>G
|
ENSP00000359244.2:n.2241+161T>G
|
|
ENST00000625514.2:c.2205+161T>G
|
ENSP00000486040.1:n.2205+161T>G
|
|
ENST00000626839.2:c.2324T>G
|
ENSP00000486706.1:p.Val775Gly
|
|
ENST00000629241.2:c.2133+161T>G
|
ENSP00000487142.1:n.2133+161T>G
|
|
ENST00000629676.2:c.1680-6042T>G
|
ENSP00000486194.1:n.1680-6042T>G
|
|
NM_004518.4:c.2294T>G
|
NP_004509.2:p.Val765Gly
|
|
NM_172106.1:c.2324T>G
|
NP_742104.1:p.Val775Gly
|
|
NM_172107.2:c.2378T>G
|
NP_742105.1:p.Val793Gly
|
|
NM_172108.3:c.2285T>G
|
NP_742106.1:p.Val762Gly
|
|
XM_006723787.1:c.2420T>G
|
XP_006723850.1:p.Val807Gly
|
|
XM_011528807.1:c.2486T>G
|
XP_011527109.1:p.Val829Gly
|
|
XM_011528808.1:c.2483T>G
|
XP_011527110.1:p.Val828Gly
|
|
XM_011528809.1:c.2456T>G
|
XP_011527111.1:p.Val819Gly
|
|
XM_011528810.1:c.2432T>G
|
XP_011527112.1:p.Val811Gly
|
|
XM_011528811.1:c.2402T>G
|
XP_011527113.1:p.Val801Gly
|
|
XM_011528812.1:c.2375T>G
|
XP_011527114.1:p.Val792Gly
|
|
XM_011528813.1:c.2360T>G
|
XP_011527115.1:p.Val787Gly
|
|
XM_011528814.1:c.1967T>G
|
XP_011527116.1:p.Val656Gly
|
|
NM_004518.5:c.2294T>G
|
NP_004509.2:p.Val765Gly
|
|
NM_172106.2:c.2324T>G
|
NP_742104.1:p.Val775Gly
|
|
NM_172107.3:c.2378T>G
|
NP_742105.1:p.Val793Gly
|
|
NM_172108.4:c.2285T>G
|
NP_742106.1:p.Val762Gly
|
|
XM_011528810.2:c.2432T>G
|
XP_011527112.1:p.Val811Gly
|
|
XM_011528811.2:c.2402T>G
|
XP_011527113.1:p.Val801Gly
|
|
XM_017027841.2:c.2429T>G
|
XP_016883330.1:p.Val810Gly
|
|
XM_017027842.2:c.2366T>G
|
XP_016883331.1:p.Val789Gly
|
|
XM_017027843.1:c.2363T>G
|
XP_016883332.1:p.Val788Gly
|
|
XM_017027844.2:c.2321T>G
|
XP_016883333.1:p.Val774Gly
|
|
XM_017027845.1:c.1394T>G
|
XP_016883334.1:p.Val465Gly
|
|
NM_004518.6:c.2294T>G
|
NP_004509.2:p.Val765Gly
|
|
NM_172106.3:c.2324T>G
|
NP_742104.1:p.Val775Gly
|
|
NM_172107.4:c.2378T>G
MANE Select
|
NP_742105.1:p.Val793Gly
|
|
NM_172108.5:c.2285T>G
|
NP_742106.1:p.Val762Gly
|
|
NM_001382235.1:c.2432T>G
|
NP_001369164.1:p.Val811Gly
|
|