ENST00000706989.1:c.2513G>A
|
ENSP00000516702.1:p.Cys838Tyr
|
|
ENST00000359125.7:c.2459G>A
MANE Select
|
ENSP00000352035.2:p.Cys820Tyr
|
|
ENST00000637193.1:c.1856G>A
|
ENSP00000490734.1:p.Cys619Tyr
|
|
ENST00000344462.8:c.2366G>A
|
ENSP00000339611.4:p.Cys789Tyr
|
|
ENST00000357249.6:c.2027G>A
|
ENSP00000349789.3:p.Cys676Tyr
|
|
ENST00000359125.6:c.2459G>A
|
ENSP00000352035.2:p.Cys820Tyr
|
|
ENST00000360480.7:c.2375G>A
|
ENSP00000353668.3:p.Cys792Tyr
|
|
ENST00000370224.5:c.2241+242G>A
|
ENSP00000359244.2:n.2241+242G>A
|
|
ENST00000625514.2:c.2205+242G>A
|
ENSP00000486040.1:n.2205+242G>A
|
|
ENST00000626839.2:c.2405G>A
|
ENSP00000486706.1:p.Cys802Tyr
|
|
ENST00000629241.2:c.2133+242G>A
|
ENSP00000487142.1:n.2133+242G>A
|
|
ENST00000629676.2:c.1680-5961G>A
|
ENSP00000486194.1:n.1680-5961G>A
|
|
NM_004518.4:c.2375G>A
|
NP_004509.2:p.Cys792Tyr
|
|
NM_172106.1:c.2405G>A
|
NP_742104.1:p.Cys802Tyr
|
|
NM_172107.2:c.2459G>A
|
NP_742105.1:p.Cys820Tyr
|
|
NM_172108.3:c.2366G>A
|
NP_742106.1:p.Cys789Tyr
|
|
XM_006723787.1:c.2501G>A
|
XP_006723850.1:p.Cys834Tyr
|
|
XM_011528807.1:c.2567G>A
|
XP_011527109.1:p.Cys856Tyr
|
|
XM_011528808.1:c.2564G>A
|
XP_011527110.1:p.Cys855Tyr
|
|
XM_011528809.1:c.2537G>A
|
XP_011527111.1:p.Cys846Tyr
|
|
XM_011528810.1:c.2513G>A
|
XP_011527112.1:p.Cys838Tyr
|
|
XM_011528811.1:c.2483G>A
|
XP_011527113.1:p.Cys828Tyr
|
|
XM_011528812.1:c.2456G>A
|
XP_011527114.1:p.Cys819Tyr
|
|
XM_011528813.1:c.2441G>A
|
XP_011527115.1:p.Cys814Tyr
|
|
XM_011528814.1:c.2048G>A
|
XP_011527116.1:p.Cys683Tyr
|
|
NM_004518.5:c.2375G>A
|
NP_004509.2:p.Cys792Tyr
|
|
NM_172106.2:c.2405G>A
|
NP_742104.1:p.Cys802Tyr
|
|
NM_172107.3:c.2459G>A
|
NP_742105.1:p.Cys820Tyr
|
|
NM_172108.4:c.2366G>A
|
NP_742106.1:p.Cys789Tyr
|
|
XM_011528810.2:c.2513G>A
|
XP_011527112.1:p.Cys838Tyr
|
|
XM_011528811.2:c.2483G>A
|
XP_011527113.1:p.Cys828Tyr
|
|
XM_017027841.2:c.2510G>A
|
XP_016883330.1:p.Cys837Tyr
|
|
XM_017027842.2:c.2447G>A
|
XP_016883331.1:p.Cys816Tyr
|
|
XM_017027843.1:c.2444G>A
|
XP_016883332.1:p.Cys815Tyr
|
|
XM_017027844.2:c.2402G>A
|
XP_016883333.1:p.Cys801Tyr
|
|
XM_017027845.1:c.1475G>A
|
XP_016883334.1:p.Cys492Tyr
|
|
NM_004518.6:c.2375G>A
|
NP_004509.2:p.Cys792Tyr
|
|
NM_172106.3:c.2405G>A
|
NP_742104.1:p.Cys802Tyr
|
|
NM_172107.4:c.2459G>A
MANE Select
|
NP_742105.1:p.Cys820Tyr
|
|
NM_172108.5:c.2366G>A
|
NP_742106.1:p.Cys789Tyr
|
|
NM_001382235.1:c.2513G>A
|
NP_001369164.1:p.Cys838Tyr
|
|