ENST00000706989.1:c.2389G=
|
ENSP00000516702.1:p.Gly797=
|
|
ENST00000359125.7:c.2335G=
MANE Select
|
ENSP00000352035.2:p.Gly779=
|
|
ENST00000637193.1:c.1732G=
|
ENSP00000490734.1:p.Gly578=
|
|
ENST00000344462.8:c.2242G=
|
ENSP00000339611.4:p.Gly748=
|
|
ENST00000357249.6:c.1903G=
|
ENSP00000349789.3:p.Gly635=
|
|
ENST00000359125.6:c.2335G=
|
ENSP00000352035.2:p.Gly779=
|
|
ENST00000360480.7:c.2251G=
|
ENSP00000353668.3:p.Gly751=
|
|
ENST00000370224.5:c.2241+118G=
|
ENSP00000359244.2:n.2241+118G=
|
|
ENST00000625514.2:c.2205+118G=
|
ENSP00000486040.1:n.2205+118G=
|
|
ENST00000626839.2:c.2281G=
|
ENSP00000486706.1:p.Gly761=
|
|
ENST00000629241.2:c.2133+118G=
|
ENSP00000487142.1:n.2133+118G=
|
|
ENST00000629676.2:c.1680-6085G=
|
ENSP00000486194.1:n.1680-6085G=
|
|
NM_004518.4:c.2251G=
|
NP_004509.2:p.Gly751=
|
|
NM_172106.1:c.2281G=
|
NP_742104.1:p.Gly761=
|
|
NM_172107.2:c.2335G=
|
NP_742105.1:p.Gly779=
|
|
NM_172108.3:c.2242G=
|
NP_742106.1:p.Gly748=
|
|
XM_006723787.1:c.2377G=
|
XP_006723850.1:p.Gly793=
|
|
XM_011528807.1:c.2443G=
|
XP_011527109.1:p.Gly815=
|
|
XM_011528808.1:c.2440G=
|
XP_011527110.1:p.Gly814=
|
|
XM_011528809.1:c.2413G=
|
XP_011527111.1:p.Gly805=
|
|
XM_011528810.1:c.2389G=
|
XP_011527112.1:p.Gly797=
|
|
XM_011528811.1:c.2359G=
|
XP_011527113.1:p.Gly787=
|
|
XM_011528812.1:c.2332G=
|
XP_011527114.1:p.Gly778=
|
|
XM_011528813.1:c.2317G=
|
XP_011527115.1:p.Gly773=
|
|
XM_011528814.1:c.1924G=
|
XP_011527116.1:p.Gly642=
|
|
NM_004518.5:c.2251G=
|
NP_004509.2:p.Gly751=
|
|
NM_172106.2:c.2281G=
|
NP_742104.1:p.Gly761=
|
|
NM_172107.3:c.2335G=
|
NP_742105.1:p.Gly779=
|
|
NM_172108.4:c.2242G=
|
NP_742106.1:p.Gly748=
|
|
XM_011528810.2:c.2389G=
|
XP_011527112.1:p.Gly797=
|
|
XM_011528811.2:c.2359G=
|
XP_011527113.1:p.Gly787=
|
|
XM_017027841.2:c.2386G=
|
XP_016883330.1:p.Gly796=
|
|
XM_017027842.2:c.2323G=
|
XP_016883331.1:p.Gly775=
|
|
XM_017027843.1:c.2320G=
|
XP_016883332.1:p.Gly774=
|
|
XM_017027844.2:c.2278G=
|
XP_016883333.1:p.Gly760=
|
|
XM_017027845.1:c.1351G=
|
XP_016883334.1:p.Gly451=
|
|
NM_004518.6:c.2251G=
|
NP_004509.2:p.Gly751=
|
|
NM_172106.3:c.2281G=
|
NP_742104.1:p.Gly761=
|
|
NM_172107.4:c.2335G=
MANE Select
|
NP_742105.1:p.Gly779=
|
|
NM_172108.5:c.2242G=
|
NP_742106.1:p.Gly748=
|
|
NM_001382235.1:c.2389G=
|
NP_001369164.1:p.Gly797=
|
|