ENST00000706989.1:c.2319C>G
|
ENSP00000516702.1:p.Tyr773Ter
|
|
ENST00000359125.7:c.2265C>G
MANE Select
|
ENSP00000352035.2:p.Tyr755Ter
|
|
ENST00000637193.1:c.1662C>G
|
ENSP00000490734.1:p.Tyr554Ter
|
|
ENST00000344462.8:c.2172C>G
|
ENSP00000339611.4:p.Tyr724Ter
|
|
ENST00000357249.6:c.1833C>G
|
ENSP00000349789.3:p.Tyr611Ter
|
|
ENST00000359125.6:c.2265C>G
|
ENSP00000352035.2:p.Tyr755Ter
|
|
ENST00000360480.7:c.2181C>G
|
ENSP00000353668.3:p.Tyr727Ter
|
|
ENST00000370224.5:c.2241+48C>G
|
ENSP00000359244.2:n.2241+48C>G
|
|
ENST00000625514.2:c.2205+48C>G
|
ENSP00000486040.1:n.2205+48C>G
|
|
ENST00000626839.2:c.2211C>G
|
ENSP00000486706.1:p.Tyr737Ter
|
|
ENST00000629241.2:c.2133+48C>G
|
ENSP00000487142.1:n.2133+48C>G
|
|
ENST00000629676.2:c.1680-6155C>G
|
ENSP00000486194.1:n.1680-6155C>G
|
|
NM_004518.4:c.2181C>G
|
NP_004509.2:p.Tyr727Ter
|
|
NM_172106.1:c.2211C>G
|
NP_742104.1:p.Tyr737Ter
|
|
NM_172107.2:c.2265C>G
|
NP_742105.1:p.Tyr755Ter
|
|
NM_172108.3:c.2172C>G
|
NP_742106.1:p.Tyr724Ter
|
|
XM_006723787.1:c.2307C>G
|
XP_006723850.1:p.Tyr769Ter
|
|
XM_011528807.1:c.2373C>G
|
XP_011527109.1:p.Tyr791Ter
|
|
XM_011528808.1:c.2370C>G
|
XP_011527110.1:p.Tyr790Ter
|
|
XM_011528809.1:c.2343C>G
|
XP_011527111.1:p.Tyr781Ter
|
|
XM_011528810.1:c.2319C>G
|
XP_011527112.1:p.Tyr773Ter
|
|
XM_011528811.1:c.2289C>G
|
XP_011527113.1:p.Tyr763Ter
|
|
XM_011528812.1:c.2262C>G
|
XP_011527114.1:p.Tyr754Ter
|
|
XM_011528813.1:c.2247C>G
|
XP_011527115.1:p.Tyr749Ter
|
|
XM_011528814.1:c.1854C>G
|
XP_011527116.1:p.Tyr618Ter
|
|
NM_004518.5:c.2181C>G
|
NP_004509.2:p.Tyr727Ter
|
|
NM_172106.2:c.2211C>G
|
NP_742104.1:p.Tyr737Ter
|
|
NM_172107.3:c.2265C>G
|
NP_742105.1:p.Tyr755Ter
|
|
NM_172108.4:c.2172C>G
|
NP_742106.1:p.Tyr724Ter
|
|
XM_011528810.2:c.2319C>G
|
XP_011527112.1:p.Tyr773Ter
|
|
XM_011528811.2:c.2289C>G
|
XP_011527113.1:p.Tyr763Ter
|
|
XM_017027841.2:c.2316C>G
|
XP_016883330.1:p.Tyr772Ter
|
|
XM_017027842.2:c.2253C>G
|
XP_016883331.1:p.Tyr751Ter
|
|
XM_017027843.1:c.2250C>G
|
XP_016883332.1:p.Tyr750Ter
|
|
XM_017027844.2:c.2208C>G
|
XP_016883333.1:p.Tyr736Ter
|
|
XM_017027845.1:c.1281C>G
|
XP_016883334.1:p.Tyr427Ter
|
|
NM_004518.6:c.2181C>G
|
NP_004509.2:p.Tyr727Ter
|
|
NM_172106.3:c.2211C>G
|
NP_742104.1:p.Tyr737Ter
|
|
NM_172107.4:c.2265C>G
MANE Select
|
NP_742105.1:p.Tyr755Ter
|
|
NM_172108.5:c.2172C>G
|
NP_742106.1:p.Tyr724Ter
|
|
NM_001382235.1:c.2319C>G
|
NP_001369164.1:p.Tyr773Ter
|
|