ENST00000706989.1:c.2472C>G
|
ENSP00000516702.1:p.Ser824Arg
|
|
ENST00000359125.7:c.2418C>G
MANE Select
|
ENSP00000352035.2:p.Ser806Arg
|
|
ENST00000637193.1:c.1815C>G
|
ENSP00000490734.1:p.Ser605Arg
|
|
ENST00000344462.8:c.2325C>G
|
ENSP00000339611.4:p.Ser775Arg
|
|
ENST00000357249.6:c.1986C>G
|
ENSP00000349789.3:p.Ser662Arg
|
|
ENST00000359125.6:c.2418C>G
|
ENSP00000352035.2:p.Ser806Arg
|
|
ENST00000360480.7:c.2334C>G
|
ENSP00000353668.3:p.Ser778Arg
|
|
ENST00000370224.5:c.2241+201C>G
|
ENSP00000359244.2:n.2241+201C>G
|
|
ENST00000625514.2:c.2205+201C>G
|
ENSP00000486040.1:n.2205+201C>G
|
|
ENST00000626839.2:c.2364C>G
|
ENSP00000486706.1:p.Ser788Arg
|
|
ENST00000629241.2:c.2133+201C>G
|
ENSP00000487142.1:n.2133+201C>G
|
|
ENST00000629676.2:c.1680-6002C>G
|
ENSP00000486194.1:n.1680-6002C>G
|
|
NM_004518.4:c.2334C>G
|
NP_004509.2:p.Ser778Arg
|
|
NM_172106.1:c.2364C>G
|
NP_742104.1:p.Ser788Arg
|
|
NM_172107.2:c.2418C>G
|
NP_742105.1:p.Ser806Arg
|
|
NM_172108.3:c.2325C>G
|
NP_742106.1:p.Ser775Arg
|
|
XM_006723787.1:c.2460C>G
|
XP_006723850.1:p.Ser820Arg
|
|
XM_011528807.1:c.2526C>G
|
XP_011527109.1:p.Ser842Arg
|
|
XM_011528808.1:c.2523C>G
|
XP_011527110.1:p.Ser841Arg
|
|
XM_011528809.1:c.2496C>G
|
XP_011527111.1:p.Ser832Arg
|
|
XM_011528810.1:c.2472C>G
|
XP_011527112.1:p.Ser824Arg
|
|
XM_011528811.1:c.2442C>G
|
XP_011527113.1:p.Ser814Arg
|
|
XM_011528812.1:c.2415C>G
|
XP_011527114.1:p.Ser805Arg
|
|
XM_011528813.1:c.2400C>G
|
XP_011527115.1:p.Ser800Arg
|
|
XM_011528814.1:c.2007C>G
|
XP_011527116.1:p.Ser669Arg
|
|
NM_004518.5:c.2334C>G
|
NP_004509.2:p.Ser778Arg
|
|
NM_172106.2:c.2364C>G
|
NP_742104.1:p.Ser788Arg
|
|
NM_172107.3:c.2418C>G
|
NP_742105.1:p.Ser806Arg
|
|
NM_172108.4:c.2325C>G
|
NP_742106.1:p.Ser775Arg
|
|
XM_011528810.2:c.2472C>G
|
XP_011527112.1:p.Ser824Arg
|
|
XM_011528811.2:c.2442C>G
|
XP_011527113.1:p.Ser814Arg
|
|
XM_017027841.2:c.2469C>G
|
XP_016883330.1:p.Ser823Arg
|
|
XM_017027842.2:c.2406C>G
|
XP_016883331.1:p.Ser802Arg
|
|
XM_017027843.1:c.2403C>G
|
XP_016883332.1:p.Ser801Arg
|
|
XM_017027844.2:c.2361C>G
|
XP_016883333.1:p.Ser787Arg
|
|
XM_017027845.1:c.1434C>G
|
XP_016883334.1:p.Ser478Arg
|
|
NM_004518.6:c.2334C>G
|
NP_004509.2:p.Ser778Arg
|
|
NM_172106.3:c.2364C>G
|
NP_742104.1:p.Ser788Arg
|
|
NM_172107.4:c.2418C>G
MANE Select
|
NP_742105.1:p.Ser806Arg
|
|
NM_172108.5:c.2325C>G
|
NP_742106.1:p.Ser775Arg
|
|
NM_001382235.1:c.2472C>G
|
NP_001369164.1:p.Ser824Arg
|
|